62 Iqvia jobs in the United Kingdom
Site Contract Associate - IQVIA Biotech - Multilingual based in EMEA
Reading, South East
IQVIA
Posted 10 days ago
Job Viewed
Job Description
**Job Overview**
Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor's requirements.
**Essential Functions**
- Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.
- Develop contract language, payment language and budget templates as required as applicable to the position
- utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
- Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
- Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
- Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
- Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
- Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements
- report contracting performance metrics and out of scope contracting activities as required.
- Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required.
- Deliver presentations to clients as required. As applicable, eEnsure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.
- May take a proactive role in developing long standing relationships with preferred IQVIA clients/customers.
**Qualifications**
- Bachelor's Degree Related field Req
- 5 year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/ore regional experience acting as a contract negotiator. Equivalent combination of education, training and experience.
- Good negotiating and communication skills with ability to challenge.
- Good interpersonal skills and a strong team player.
- Strong legal, financial and/or technical writing skills.
- Strong understanding of regulated clinical trial environment and knowledge of drug development process.
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
- Knowledge of applicable regulatory requirements, SOPs and company's Corporate Standards.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor's requirements.
**Essential Functions**
- Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.
- Develop contract language, payment language and budget templates as required as applicable to the position
- utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
- Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
- Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
- Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
- Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
- Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements
- report contracting performance metrics and out of scope contracting activities as required.
- Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required.
- Deliver presentations to clients as required. As applicable, eEnsure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.
- May take a proactive role in developing long standing relationships with preferred IQVIA clients/customers.
**Qualifications**
- Bachelor's Degree Related field Req
- 5 year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/ore regional experience acting as a contract negotiator. Equivalent combination of education, training and experience.
- Good negotiating and communication skills with ability to challenge.
- Good interpersonal skills and a strong team player.
- Strong legal, financial and/or technical writing skills.
- Strong understanding of regulated clinical trial environment and knowledge of drug development process.
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
- Knowledge of applicable regulatory requirements, SOPs and company's Corporate Standards.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
0
Senior Site Contract Associate - IQVIA Biotech - Multilingual based in EMEA
Reading, South East
IQVIA
Posted 10 days ago
Job Viewed
Job Description
**Job Overview**
Manage the contract strategy and support delivery of all required start-up contracting activities for selected sponsors and for complex studies or multi-protocol programs as determined by the Sponsor's requirements.
**Essential Functions**
- Responsible for the development of complex investigator grant estimates, contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.
- Develop contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors and complex studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy, as applicable to the position.
- Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
- Provide specialist legal, operational and financial contracting support to the study teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of complex clinical trials, whilst ensuring compliance with regulatory requirements and local laws.
- Create, publish and/or review core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
- Assess and review the contracting landscape and contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
- Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements report contracting performance metrics and out of scope contracting activities as required.
- Work with Quality Management to ensure appropriate contract management and quality standards.
- As applicable, ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.
**Qualifications**
- Bachelor's Degree Related field
- 4 to 7 years' relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable experience acting as an international contract expert.
- Good negotiating and communication skills with ability to challenge.
- Thorough understanding of regulated clinical trial environment and knowledge of drug development process.
- Proven ability to exercise independent judgment, taking calculated risks when making decisions.
- Strong knowledge of clinical trial contract management.
- Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
- Ability to utilize metrics and then communicate these with study team to establish timelines for deliverables.
- Proven ability to take on a project or new initiative and grow the program to make an impact across departments.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Manage the contract strategy and support delivery of all required start-up contracting activities for selected sponsors and for complex studies or multi-protocol programs as determined by the Sponsor's requirements.
**Essential Functions**
- Responsible for the development of complex investigator grant estimates, contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.
- Develop contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors and complex studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy, as applicable to the position.
- Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
- Provide specialist legal, operational and financial contracting support to the study teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of complex clinical trials, whilst ensuring compliance with regulatory requirements and local laws.
- Create, publish and/or review core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
- Assess and review the contracting landscape and contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
- Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements report contracting performance metrics and out of scope contracting activities as required.
- Work with Quality Management to ensure appropriate contract management and quality standards.
- As applicable, ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.
**Qualifications**
- Bachelor's Degree Related field
- 4 to 7 years' relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable experience acting as an international contract expert.
- Good negotiating and communication skills with ability to challenge.
- Thorough understanding of regulated clinical trial environment and knowledge of drug development process.
- Proven ability to exercise independent judgment, taking calculated risks when making decisions.
- Strong knowledge of clinical trial contract management.
- Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
- Ability to utilize metrics and then communicate these with study team to establish timelines for deliverables.
- Proven ability to take on a project or new initiative and grow the program to make an impact across departments.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
1
Strategic Communications Consultant (Sr Account Manager) - Arc Bio Communications (IQVIA) - UK
London, London
IQVIA
Posted 10 days ago
Job Viewed
Job Description
_The role can be hybrid or remote._
**About us**
Arc Bio Communications is passionate about delivering global communications strategies for biopharmaceutical and biotechnology companies that add value and bring innovations to life. Our unique approach blends the strategic rigour of management consultancy, the scientific expertise of medical education, and the creativity and reach of communications.
In 2024, we joined forces with IQVIA, to expand our global capabilities and influence even further.
Are you passionate about bringing game-changing healthcare innovation to life through strategic thinking?
Find out more about us here: you**
A highly experienced healthcare communications consultant with a minimum of 8 years' experience in public relations, medical communications and/or scientific communications. You have relevant experience in:
+ Developing effective scientific or communications strategies and solutions aligned to the client's business objectives
+ Challenging and interrogating client briefs through structured questioning and an understanding of the client and external landscape
+ Producing strategically aligned high-quality communications / scientific content (e.g. narratives, scientific platforms, messaging, senior leader presentations, articles, social content)
+ Effectively leading, motivating and inspiring account teams to deliver communications programmes and projects of high strategic value
+ Building and maintaining strong client relationships
+ Effectively engaging with senior level pharmaceutical executives
+ Growing business both organically through existing client relationships or supporting with new business opportunities and proposals
+ Accurate financial planning, management, forecasting and team resourcing
**About the role**
**Client service:**
+ Leads, builds and maintains excellent relationships with clients and provides them ongoing consultation and counsel on a peer-to-peer basis.
+ Develops strong and effective scientific and/ or corporate communications strategies and solutions in service of client objectives. Always regards the client's challenges as unique, never generic, and a shared journey between them and Arc Bio. Unafraid of ambiguity and able to ask probing questions to get to the heart of a client brief.
+ Produces client-ready work of the highest standard, always delivered with exceptional quality standards, in an efficient and timely manner.
+ Develops high quality business proposals for both new and existing clients.
+ Works consistently to grow existing accounts organically through high quality work and ongoing discussions with clients.
+ Networks outside of Arc Bio to support new business development identifying business leads and representing Arc Bio at industry events.
**Project Management:**
+ Sets up relevant systems and process to facilitate accurate programme/project planning and management. Able to effectively and quickly course correct if challenges arise.
+ Produces accurate cost estimates and controls budgets efficiently and carefully whilst keeping clients and team fully informed of eventual or possible overspend, providing relevant solutions where necessary.
**Leadership:**
+ Effectively leads client account teams setting the strategy (in partnership with Arc Bio Partners and clients), proactively reviews and evaluates progress, course correcting where necessary.
+ Effectively delegates and prioritises within client account teams, providing direction to ensure delivery whilst providing ownership.
+ Demonstrates ability to develop others and provide direction and feedback tailored to the skill level of team members.
+ Drives communication between teams and the client and takes ownership of strategic client discussions vs day-to-day delivery.
**Communication and impact:**
+ Always presents with confidence and conviction.
+ Demonstrates the ability to influence, negotiate and overcome objections from senior stakeholders.
+ Effectively adapts communication style to suit different audiences and to gain buy in.
+ Thinks clearly and quickly, always has a professional point of view and provides ad hoc client counsel.
+ Demonstrates ability to develop others and provide direction and feedback tailored to skill level of team members.
**About technical ability and skills**
**Industry:**
+ Keeps up to date with factors influencing the pharma and biotech sectors.
+ Understands the mechanics underpinning industry sector activities and has a competent knowledge of the basics of business e.g. factors influencing company valuations, fundamental financial definitions and mechanisms.
+ Engages in industry "scanning" and maintains a strong current knowledge of industry opportunities and developments and our clients' operating environment.
**Scientific:**
+ Has a strong working knowledge of the science covering our clients' areas of focus.
+ Has an ongoing commitment to deepening and expanding knowledge in modalities, modes of action, epidemiology, clinical trial design and anything else that may be relevant to strategic planning and advice, both from the point of view of the client and their competitor environment.
+ In chosen areas of specialism (scientific or strategic), is capable of constructively challenging client thinking on a peer-to-peer level, producing novel points of view to help clients view potential solutions from new angles where appropriate and useful.
**Strategy:**
+ Can confidently discuss strategy in reference to client goals and objectives.
+ Understands theoretical approaches and models used in strategy and communications consulting and applies these to client challenges.
+ Is a keen student of the evolving strategic communications environment (including new tools and models, and their strengths and limitations). Takes an active role in strategic development and strategic workshop facilitation.
**Marketing and communications:**
+ Understands the fundamental principles of healthcare marketing and communications, with a strong capabilities in public relations, medical education and/or scientific communications.
+ Understands means of evaluation and KPIs across communications channels.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**About us**
Arc Bio Communications is passionate about delivering global communications strategies for biopharmaceutical and biotechnology companies that add value and bring innovations to life. Our unique approach blends the strategic rigour of management consultancy, the scientific expertise of medical education, and the creativity and reach of communications.
In 2024, we joined forces with IQVIA, to expand our global capabilities and influence even further.
Are you passionate about bringing game-changing healthcare innovation to life through strategic thinking?
Find out more about us here: you**
A highly experienced healthcare communications consultant with a minimum of 8 years' experience in public relations, medical communications and/or scientific communications. You have relevant experience in:
+ Developing effective scientific or communications strategies and solutions aligned to the client's business objectives
+ Challenging and interrogating client briefs through structured questioning and an understanding of the client and external landscape
+ Producing strategically aligned high-quality communications / scientific content (e.g. narratives, scientific platforms, messaging, senior leader presentations, articles, social content)
+ Effectively leading, motivating and inspiring account teams to deliver communications programmes and projects of high strategic value
+ Building and maintaining strong client relationships
+ Effectively engaging with senior level pharmaceutical executives
+ Growing business both organically through existing client relationships or supporting with new business opportunities and proposals
+ Accurate financial planning, management, forecasting and team resourcing
**About the role**
**Client service:**
+ Leads, builds and maintains excellent relationships with clients and provides them ongoing consultation and counsel on a peer-to-peer basis.
+ Develops strong and effective scientific and/ or corporate communications strategies and solutions in service of client objectives. Always regards the client's challenges as unique, never generic, and a shared journey between them and Arc Bio. Unafraid of ambiguity and able to ask probing questions to get to the heart of a client brief.
+ Produces client-ready work of the highest standard, always delivered with exceptional quality standards, in an efficient and timely manner.
+ Develops high quality business proposals for both new and existing clients.
+ Works consistently to grow existing accounts organically through high quality work and ongoing discussions with clients.
+ Networks outside of Arc Bio to support new business development identifying business leads and representing Arc Bio at industry events.
**Project Management:**
+ Sets up relevant systems and process to facilitate accurate programme/project planning and management. Able to effectively and quickly course correct if challenges arise.
+ Produces accurate cost estimates and controls budgets efficiently and carefully whilst keeping clients and team fully informed of eventual or possible overspend, providing relevant solutions where necessary.
**Leadership:**
+ Effectively leads client account teams setting the strategy (in partnership with Arc Bio Partners and clients), proactively reviews and evaluates progress, course correcting where necessary.
+ Effectively delegates and prioritises within client account teams, providing direction to ensure delivery whilst providing ownership.
+ Demonstrates ability to develop others and provide direction and feedback tailored to the skill level of team members.
+ Drives communication between teams and the client and takes ownership of strategic client discussions vs day-to-day delivery.
**Communication and impact:**
+ Always presents with confidence and conviction.
+ Demonstrates the ability to influence, negotiate and overcome objections from senior stakeholders.
+ Effectively adapts communication style to suit different audiences and to gain buy in.
+ Thinks clearly and quickly, always has a professional point of view and provides ad hoc client counsel.
+ Demonstrates ability to develop others and provide direction and feedback tailored to skill level of team members.
**About technical ability and skills**
**Industry:**
+ Keeps up to date with factors influencing the pharma and biotech sectors.
+ Understands the mechanics underpinning industry sector activities and has a competent knowledge of the basics of business e.g. factors influencing company valuations, fundamental financial definitions and mechanisms.
+ Engages in industry "scanning" and maintains a strong current knowledge of industry opportunities and developments and our clients' operating environment.
**Scientific:**
+ Has a strong working knowledge of the science covering our clients' areas of focus.
+ Has an ongoing commitment to deepening and expanding knowledge in modalities, modes of action, epidemiology, clinical trial design and anything else that may be relevant to strategic planning and advice, both from the point of view of the client and their competitor environment.
+ In chosen areas of specialism (scientific or strategic), is capable of constructively challenging client thinking on a peer-to-peer level, producing novel points of view to help clients view potential solutions from new angles where appropriate and useful.
**Strategy:**
+ Can confidently discuss strategy in reference to client goals and objectives.
+ Understands theoretical approaches and models used in strategy and communications consulting and applies these to client challenges.
+ Is a keen student of the evolving strategic communications environment (including new tools and models, and their strengths and limitations). Takes an active role in strategic development and strategic workshop facilitation.
**Marketing and communications:**
+ Understands the fundamental principles of healthcare marketing and communications, with a strong capabilities in public relations, medical education and/or scientific communications.
+ Understands means of evaluation and KPIs across communications channels.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
2
Sr Strategic Communications Consultant (Sr Account Director) - Arc Bio Communications, (IQVIA) - UK
London, London
IQVIA
Posted 10 days ago
Job Viewed
Job Description
**About us**
Arc Bio Communications is passionate about delivering global communications strategies for biopharmaceutical and biotechnology companies that add value and bring innovations to life. Our unique approach blends the strategic rigour of management consultancy, the scientific expertise of medical education, and the creativity and reach of communications.
In 2024, we joined forces with IQVIA, to expand our global capabilities and influence even further.
Are you passionate about bringing game-changing healthcare innovation to life through strategic thinking?
Find out more about us here: you**
A highly experienced healthcare communications consultant with a minimum of 8 years' experience in public relations, medical communications and/or scientific communications. You have relevant experience in:
+ Developing effective scientific or communications strategies and solutions aligned to the client's business objectives
+ Challenging and interrogating client briefs through structured questioning and an understanding of the client and external landscape
+ Producing strategically aligned high-quality communications / scientific content (e.g. narratives, scientific platforms, messaging, senior leader presentations, articles, social content)
+ Effectively leading, motivating and inspiring account teams to deliver communications programmes and projects of high strategic value
+ Building and maintaining strong client relationships
+ Effectively engaging with senior level pharmaceutical executives
+ Growing business both organically through existing client relationships or supporting with new business opportunities and proposals
+ Accurate financial planning, management, forecasting and team resourcing
**About the role**
**Client service:**
+ Leads, builds and maintains excellent relationships with clients and provides them ongoing consultation and counsel on a peer-to-peer basis.
+ Develops strong and effective scientific and/ or corporate communications strategies and solutions in service of client objectives. Always regards the client's challenges as unique, never generic, and a shared journey between them and Arc Bio. Unafraid of ambiguity and able to ask probing questions to get to the heart of a client brief.
+ Produces client-ready work of the highest standard, always delivered with exceptional quality standards, in an efficient and timely manner.
+ Develops high quality business proposals for both new and existing clients.
+ Works consistently to grow existing accounts organically through high quality work and ongoing discussions with clients.
+ Networks outside of Arc Bio to support new business development identifying business leads and representing Arc Bio at industry events.
**Project Management:**
+ Sets up relevant systems and process to facilitate accurate programme/project planning and management. Able to effectively and quickly course correct if challenges arise.
+ Produces accurate cost estimates and controls budgets efficiently and carefully whilst keeping clients and team fully informed of eventual or possible overspend, providing relevant solutions where necessary.
**Leadership:**
+ Effectively leads client account teams setting the strategy (in partnership with Arc Bio Partners and clients), proactively reviews and evaluates progress, course correcting where necessary.
+ Effectively delegates and prioritises within client account teams, providing direction to ensure delivery whilst providing ownership.
+ Demonstrates ability to develop others and provide direction and feedback tailored to the skill level of team members.
+ Drives communication between teams and the client and takes ownership of strategic client discussions vs day-to-day delivery.
**Communication and impact:**
+ Always presents with confidence and conviction.
+ Demonstrates the ability to influence, negotiate and overcome objections from senior stakeholders.
+ Effectively adapts communication style to suit different audiences and to gain buy in.
+ Thinks clearly and quickly, always has a professional point of view and provides ad hoc client counsel.
+ Demonstrates ability to develop others and provide direction and feedback tailored to skill level of team members.
**About technical ability and skills**
**Industry:**
+ Keeps up to date with factors influencing the pharma and biotech sectors.
+ Understands the mechanics underpinning industry sector activities and has a competent knowledge of the basics of business e.g. factors influencing company valuations, fundamental financial definitions and mechanisms.
+ Engages in industry "scanning" and maintains a strong current knowledge of industry opportunities and developments and our clients' operating environment.
**Scientific:**
+ Has a strong working knowledge of the science covering our clients' areas of focus.
+ Has an ongoing commitment to deepening and expanding knowledge in modalities, modes of action, epidemiology, clinical trial design and anything else that may be relevant to strategic planning and advice, both from the point of view of the client and their competitor environment.
+ In chosen areas of specialism (scientific or strategic), is capable of constructively challenging client thinking on a peer-to-peer level, producing novel points of view to help clients view potential solutions from new angles where appropriate and useful.
**Strategy:**
+ Can confidently discuss strategy in reference to client goals and objectives.
+ Understands theoretical approaches and models used in strategy and communications consulting and applies these to client challenges.
+ Is a keen student of the evolving strategic communications environment (including new tools and models, and their strengths and limitations). Takes an active role in strategic development and strategic workshop facilitation.
**Marketing and communications:**
+ Understands the fundamental principles of healthcare marketing and communications, with a strong capabilities in public relations, medical education and/or scientific communications.
+ Understands means of evaluation and KPIs across communications channels.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Arc Bio Communications is passionate about delivering global communications strategies for biopharmaceutical and biotechnology companies that add value and bring innovations to life. Our unique approach blends the strategic rigour of management consultancy, the scientific expertise of medical education, and the creativity and reach of communications.
In 2024, we joined forces with IQVIA, to expand our global capabilities and influence even further.
Are you passionate about bringing game-changing healthcare innovation to life through strategic thinking?
Find out more about us here: you**
A highly experienced healthcare communications consultant with a minimum of 8 years' experience in public relations, medical communications and/or scientific communications. You have relevant experience in:
+ Developing effective scientific or communications strategies and solutions aligned to the client's business objectives
+ Challenging and interrogating client briefs through structured questioning and an understanding of the client and external landscape
+ Producing strategically aligned high-quality communications / scientific content (e.g. narratives, scientific platforms, messaging, senior leader presentations, articles, social content)
+ Effectively leading, motivating and inspiring account teams to deliver communications programmes and projects of high strategic value
+ Building and maintaining strong client relationships
+ Effectively engaging with senior level pharmaceutical executives
+ Growing business both organically through existing client relationships or supporting with new business opportunities and proposals
+ Accurate financial planning, management, forecasting and team resourcing
**About the role**
**Client service:**
+ Leads, builds and maintains excellent relationships with clients and provides them ongoing consultation and counsel on a peer-to-peer basis.
+ Develops strong and effective scientific and/ or corporate communications strategies and solutions in service of client objectives. Always regards the client's challenges as unique, never generic, and a shared journey between them and Arc Bio. Unafraid of ambiguity and able to ask probing questions to get to the heart of a client brief.
+ Produces client-ready work of the highest standard, always delivered with exceptional quality standards, in an efficient and timely manner.
+ Develops high quality business proposals for both new and existing clients.
+ Works consistently to grow existing accounts organically through high quality work and ongoing discussions with clients.
+ Networks outside of Arc Bio to support new business development identifying business leads and representing Arc Bio at industry events.
**Project Management:**
+ Sets up relevant systems and process to facilitate accurate programme/project planning and management. Able to effectively and quickly course correct if challenges arise.
+ Produces accurate cost estimates and controls budgets efficiently and carefully whilst keeping clients and team fully informed of eventual or possible overspend, providing relevant solutions where necessary.
**Leadership:**
+ Effectively leads client account teams setting the strategy (in partnership with Arc Bio Partners and clients), proactively reviews and evaluates progress, course correcting where necessary.
+ Effectively delegates and prioritises within client account teams, providing direction to ensure delivery whilst providing ownership.
+ Demonstrates ability to develop others and provide direction and feedback tailored to the skill level of team members.
+ Drives communication between teams and the client and takes ownership of strategic client discussions vs day-to-day delivery.
**Communication and impact:**
+ Always presents with confidence and conviction.
+ Demonstrates the ability to influence, negotiate and overcome objections from senior stakeholders.
+ Effectively adapts communication style to suit different audiences and to gain buy in.
+ Thinks clearly and quickly, always has a professional point of view and provides ad hoc client counsel.
+ Demonstrates ability to develop others and provide direction and feedback tailored to skill level of team members.
**About technical ability and skills**
**Industry:**
+ Keeps up to date with factors influencing the pharma and biotech sectors.
+ Understands the mechanics underpinning industry sector activities and has a competent knowledge of the basics of business e.g. factors influencing company valuations, fundamental financial definitions and mechanisms.
+ Engages in industry "scanning" and maintains a strong current knowledge of industry opportunities and developments and our clients' operating environment.
**Scientific:**
+ Has a strong working knowledge of the science covering our clients' areas of focus.
+ Has an ongoing commitment to deepening and expanding knowledge in modalities, modes of action, epidemiology, clinical trial design and anything else that may be relevant to strategic planning and advice, both from the point of view of the client and their competitor environment.
+ In chosen areas of specialism (scientific or strategic), is capable of constructively challenging client thinking on a peer-to-peer level, producing novel points of view to help clients view potential solutions from new angles where appropriate and useful.
**Strategy:**
+ Can confidently discuss strategy in reference to client goals and objectives.
+ Understands theoretical approaches and models used in strategy and communications consulting and applies these to client challenges.
+ Is a keen student of the evolving strategic communications environment (including new tools and models, and their strengths and limitations). Takes an active role in strategic development and strategic workshop facilitation.
**Marketing and communications:**
+ Understands the fundamental principles of healthcare marketing and communications, with a strong capabilities in public relations, medical education and/or scientific communications.
+ Understands means of evaluation and KPIs across communications channels.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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3
Clinical Research Coordinator
Halifax, Yorkshire and the Humber
IQVIA
Posted 1 day ago
Job Viewed
Job Description
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.
This part-time role is to support a site in Halifax, West Yorkshire in conducting a clinical trial for 15 hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
- Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
- Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
- Plan and coordinate logistical activity for study procedures according to the study protocol
- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
- Correct custody of study drug according to site standard operating procedures
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
We are looking for candidates with the following skills and experience:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
- Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
- Basic knowledge of medical terminology
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
- Good organizational skills with the ability to pay close attention to detail.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Coordinator
Oldham, North West
IQVIA
Posted 1 day ago
Job Viewed
Job Description
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.
This part-time role is to support a site in Oldham in conducting a clinical trial for 16 hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
- Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
- Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
- Plan and coordinate logistical activity for study procedures according to the study protocol
- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
- Correct custody of study drug according to site standard operating procedures
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
We are looking for candidates with the following skills and experience:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
- Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
- Basic knowledge of medical terminology
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
- Good organizational skills with the ability to pay close attention to detail.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Coordinator
Milton Keynes, South East
Actalent
Posted 1 day ago
Job Viewed
Job Description
Job Title: Clinical Research Coordinator (Band 6 Nurse)
Contract Type: Part-Time (2–3 days/week)
Overview:
We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.
Key Responsibilities:
- Identify and recruit eligible patients for clinical trials.
- Perform accurate and timely data entry into study databases.
- Collaborate with research and clinical teams to ensure protocol compliance.
- Maintain high standards of documentation and regulatory adherence.
Requirements:
- Registered Band 6 Nurse with relevant clinical experience.
- Demonstrated experience in patient identification and data entry.
- Strong attention to detail and organizational skills.
- Must be available to work every Wednesday, plus two additional weekdays.
Please submit your CV or get in touch via email:
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Research Physician
London, London
Park Street People
Posted 8 days ago
Job Viewed
Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Physician
Park Street People
Posted 8 days ago
Job Viewed
Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Physician
Preston, North West
Planet Pharma
Posted 11 days ago
Job Viewed
Job Description
This advertiser has chosen not to accept applicants from your region.
9