354 Iqvia jobs in the United Kingdom
CRA 2, IQVIA Biotech
IQVIA
Posted 16 days ago
Job Viewed
Job Description
**Join IQVIA Biotech - Where Innovation Meets Impact**
At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won't just be part of the process-you'll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community.
If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive.
**Responsibilities**
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
- Minimum of 1 year of experience of on-site monitoring experience
- Experience monitoring Oncology studies is a must
- Bachelor's Degree in scientific discipline or health care preferred
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer, iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**This role is not eligible for UK visa sponsorship**
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
At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won't just be part of the process-you'll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community.
If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive.
**Responsibilities**
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
- Minimum of 1 year of experience of on-site monitoring experience
- Experience monitoring Oncology studies is a must
- Bachelor's Degree in scientific discipline or health care preferred
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer, iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**This role is not eligible for UK visa sponsorship**
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
CRA 2, IQVIA Biotech
Reading, South East
IQVIA
Posted 16 days ago
Job Viewed
Job Description
**Join IQVIA Biotech - Where Innovation Meets Impact**
At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won't just be part of the process-you'll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community.
If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive.
**Responsibilities**
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
- Minimum of 1 year of experience of on-site monitoring experience
- Experience monitoring Oncology studies is a must
- Bachelor's Degree in scientific discipline or health care preferred
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer, iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**This role is not eligible for UK visa sponsorship**
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
At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won't just be part of the process-you'll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community.
If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive.
**Responsibilities**
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
- Minimum of 1 year of experience of on-site monitoring experience
- Experience monitoring Oncology studies is a must
- Bachelor's Degree in scientific discipline or health care preferred
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer, iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
**This role is not eligible for UK visa sponsorship**
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
Site Contract Associate - IQVIA Biotech - UK based
Reading, South East
IQVIA
Posted 19 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.
**O** **n-site presence in the London office**
**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,
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.
**O** **n-site presence in the London office**
**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,
This advertiser has chosen not to accept applicants from your region.
2
Senior Strategic Healthcare Communications Professional - Arc Bio Communications (an IQVIA business)
London, London
IQVIA
Posted 4 days ago
Job Viewed
Job Description
A highly experienced healthcare communications leader with a minimum of 10-12 years' experience in strategic healthcare communications, medical communications and/or scientific communications. Ideally with strong consultancy/agency experience.
**Role description:**
**Client service:**
+ With intermittent Partner/Managing Partner input works to build a portfolio of business and take ownership of this within its entirety.
+ Leads, builds and sets the direction and strategy of the portfolio on a day-to-day basis.
+ Develops industry leading scientific, creative and/or commercial communication strategies and programmes.
+ Leads, builds and maintains excellent relationships with clients and provides them ongoing consultation and counsel on a peer-to-peer basis.
+ Confident at conversing directly with and providing strategic guidance to c-suite and/or senior leadership teams within pharma and biotechs.
**Business growth:**
+ Works consistently to grow existing portfolio of business organically through high quality work and identifying new work of high strategic value.
+ Has a strong professional network that can be leveraged for business development.
+ Brings in new opportunities and works to convert them to new client workstreams
+ Networks consistently outside of Arc Bio, attends and contributes to industry and client events and meetings representing Arc Bio as a brand within the industry.
**Project Management:**
+ Accountable for high-level project planning and management, effective budgetary control and resourcing/team planning to effectively delivery projects within their portfolio.
+ Effectively delegates and prioritizes for project teams, providing direction to ensure delivery whilst allowing individual ownership.
+ Provides project management guidance and training to direct teams.
+ Sets the highest standards with respect to quality, original, strong strategic thinking and detail accuracy at all times.
+ Supports and guides teams through project or client challenges.
**Leadership:**
+ Demonstrates strong leadership capability with executive presence.
+ Demonstrates ability to develop others and provide direction and feedback tailored to the skill level of team members.
+ Embraces and actions team and peer feedback as a driver for change.
+ Generates buy-in, listens openly to colleagues, recognizes contributions and ensures consistency of decisions
+ Takes accountability for their team and outcomes, encouraging their team to do the same, inspires and fosters team commitment.
+ Drives communication between teams and the client.
+ Supports, encourages and challenges colleagues in a constructive and supportive way.
+ Contributes to the development and future direction of Arc Bio alongside the Partners/Managing Partners.
+ Demonstrates and champions the Arc Bio culture.
**Communication and impact:**
+ Proven ability of presenting at a senior stakeholder and industry level.
+ Demonstrates thought leadership at a client portfolio or practice domain level.
+ 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.
**Technical ability and skills** (ABC team members should be ready to communicate on these with both knowledge and authority-strong command; of at least three of these is required at Associate Partner level and above):
Industry:
+ Keeps up to date with factors influencing the pharma and biotech sectors (including M&A activity, pharma corporate innovation strategy and the various industry head- and tail-winds).
+ Maintains a strong current knowledge of industry opportunities and developments and our clients' operating environment. Uses these findings to draw conclusions, formulate actions and exploit opportunities relevant to the Arc Bio business.
Scientific:
+ Has a strong working knowledge of the science covering our clients' areas of focus.
+ In chosen areas of scientific specialism, is capable of constructively challenging client thinking on a peer-to-peer level, producing novel scientific strategic points of view to help clients view potential solutions from new angles where appropriate and useful.
+ Keeps aware of latest announcements coming out of key congresses, key experts in the field, and any overall, rapidly-evolving trends and how these might impact communication strategy recommendations to the client.
Strategy:
+ Can confidently discuss strategy in reference to client goals and objectives.
+ Understands and applies theoretical approaches and models used in strategy consulting. Able to integrate the relevant theories into a given client challenge.
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
**Role description:**
**Client service:**
+ With intermittent Partner/Managing Partner input works to build a portfolio of business and take ownership of this within its entirety.
+ Leads, builds and sets the direction and strategy of the portfolio on a day-to-day basis.
+ Develops industry leading scientific, creative and/or commercial communication strategies and programmes.
+ Leads, builds and maintains excellent relationships with clients and provides them ongoing consultation and counsel on a peer-to-peer basis.
+ Confident at conversing directly with and providing strategic guidance to c-suite and/or senior leadership teams within pharma and biotechs.
**Business growth:**
+ Works consistently to grow existing portfolio of business organically through high quality work and identifying new work of high strategic value.
+ Has a strong professional network that can be leveraged for business development.
+ Brings in new opportunities and works to convert them to new client workstreams
+ Networks consistently outside of Arc Bio, attends and contributes to industry and client events and meetings representing Arc Bio as a brand within the industry.
**Project Management:**
+ Accountable for high-level project planning and management, effective budgetary control and resourcing/team planning to effectively delivery projects within their portfolio.
+ Effectively delegates and prioritizes for project teams, providing direction to ensure delivery whilst allowing individual ownership.
+ Provides project management guidance and training to direct teams.
+ Sets the highest standards with respect to quality, original, strong strategic thinking and detail accuracy at all times.
+ Supports and guides teams through project or client challenges.
**Leadership:**
+ Demonstrates strong leadership capability with executive presence.
+ Demonstrates ability to develop others and provide direction and feedback tailored to the skill level of team members.
+ Embraces and actions team and peer feedback as a driver for change.
+ Generates buy-in, listens openly to colleagues, recognizes contributions and ensures consistency of decisions
+ Takes accountability for their team and outcomes, encouraging their team to do the same, inspires and fosters team commitment.
+ Drives communication between teams and the client.
+ Supports, encourages and challenges colleagues in a constructive and supportive way.
+ Contributes to the development and future direction of Arc Bio alongside the Partners/Managing Partners.
+ Demonstrates and champions the Arc Bio culture.
**Communication and impact:**
+ Proven ability of presenting at a senior stakeholder and industry level.
+ Demonstrates thought leadership at a client portfolio or practice domain level.
+ 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.
**Technical ability and skills** (ABC team members should be ready to communicate on these with both knowledge and authority-strong command; of at least three of these is required at Associate Partner level and above):
Industry:
+ Keeps up to date with factors influencing the pharma and biotech sectors (including M&A activity, pharma corporate innovation strategy and the various industry head- and tail-winds).
+ Maintains a strong current knowledge of industry opportunities and developments and our clients' operating environment. Uses these findings to draw conclusions, formulate actions and exploit opportunities relevant to the Arc Bio business.
Scientific:
+ Has a strong working knowledge of the science covering our clients' areas of focus.
+ In chosen areas of scientific specialism, is capable of constructively challenging client thinking on a peer-to-peer level, producing novel scientific strategic points of view to help clients view potential solutions from new angles where appropriate and useful.
+ Keeps aware of latest announcements coming out of key congresses, key experts in the field, and any overall, rapidly-evolving trends and how these might impact communication strategy recommendations to the client.
Strategy:
+ Can confidently discuss strategy in reference to client goals and objectives.
+ Understands and applies theoretical approaches and models used in strategy consulting. Able to integrate the relevant theories into a given client challenge.
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.
3
Strategic Communications Consultant (Sr Account Manager) - Arc Bio Communications (IQVIA) - UK
London, London
IQVIA
Posted 9 days ago
Job Viewed
Job Description
_The role can be hybrid or remote._
_P_ _lease note that we're not sponsoring visas for this position._
**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
_P_ _lease note that we're not sponsoring visas for this position._
**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
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Coordinator
Milton Keynes, South East
Actalent
Posted 3 days ago
Job Viewed
Job Description
We're Hiring: Clinical Nurse
Focus Area: Multiple Myeloma Research
Are you a Band 6 Nurse with a keen eye for detail and a passion for clinical research? We're looking for someone to join our team at Milton Keynes University Hospital on a part-time basis (2–3 days/week) to support a research study in Multiple Myeloma .
What you'll be doing:
- Patient identification and recruitment
- Accurate clinical data entry
- Supporting research operations on-site
What we're looking for:
- NMC-registered Band 6 Nurse
- Experience with patient identification and clinical data entry
- Availability on Wednesdays , plus two additional weekdays
- Strong communication and organisational skills
- This is a great opportunity to contribute to impactful research while maintaining a flexible schedule.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Coordinator
Milton Keynes, South East
Actalent
Posted 22 days 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 Coordinator
Bath, South West
Actalent
Posted 1 day ago
Job Viewed
Job Description
URGENT HIRING: Clinical Research Coordinator – Bath
I'm reaching out with an exciting full-time opportunity for a Clinical Research Coordinator (CRC) to join a global clinical research service provider supporting multiple sponsors.
Therapeutic Area: Atopic Dermatitis (experience required)
Location: On-site in Bath
Start Date: ASAP
Duration: Until October (potential to extend)
This role is ideal for a Band 5/6 Nurse or Clinical Research Nurse ready to step into a CRC title.
Key Responsibilities:
- Patient identification & chart reviews
- Referral physician networking
- Community outreach
Preferred Experience:
- Background in nursing or clinical research
- Familiarity with Millennium Sauna or other EDC systems
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate
CCS-Global
Posted 1 day ago
Job Viewed
Job Description
Are you a passionate CRA II or Senior CRA looking for your next challenge?
We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusively with a leading Pharmaceutical client.
This is a unique opportunity to be part of a dynamic and supportive environment where your contributions directly impact the future of medicine. Our clients FSP model provides the stability and support of a dedicated team, while you gain exposure to the innovative research of a top-tier pharmaceutical company.
About the role:
As a CRA II or Senior CRA, you will be responsible for the full range of monitoring activities, from site initiation to close-out. You'll ensure the highest standards of data quality and compliance with ICH-GCP, protocols, and all applicable regulations. This role is home-based and will involve travel to sites across your designated region.
What our client offer:
- Salary: £45,000 - £55,000 per annum, depending on experience.
- Car/Car Allowance: A company car or a competitive car allowance.
- Bonus & Benefits: An attractive bonus scheme and a comprehensive benefits package.
- Career Growth: We are committed to your professional development and offer extensive training, mentorship, and opportunities for progression within our growing FSP.
Location:
This is a home-based role to be based in one of the following regions:
- North England
- North West England
- Midlands
- London
- South England
Requirements:
- Proven experience as a CRA, with a strong understanding of the clinical trial lifecycle. 18 months minimum as a CRA to be CRAII and 3 year + to be considered for Senior CRA.
- Excellent knowledge of ICH-GCP guidelines and relevant regulations.
- Strong communication and interpersonal skills.
- A proactive and independent approach to your work.
- A full UK driving licence and willingness to travel.
If you are ready to take the next step in your career and join a company that values growth, training, and support, we want to hear from you.
Apply now or message us for more details!
#CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate
Barrington James
Posted 1 day ago
Job Viewed
Job Description
Job Title: Freelance Clinical Research Associate – Associate Level (Oncology)
Location: Hybrid UK Based
Employment Type: Freelance
Function: Clinical Operations
Therapeutic Area: Oncology
Reports To: Clinical Operations Manager
About the Role
We are seeking a motivated and detail-oriented Freelance Clinical Research Associate (Associate Level) with a passion for oncology clinical trials. This is an exciting opportunity for an early-career CRA to gain hands-on experience in a dynamic, cross-functional research environment. You will support clinical trial activities across multiple oncology study sites, ensuring compliance with regulatory guidelines, ICH-GCP, and study protocols.
Key Responsibilities
- Conduct site monitoring visits (pre-study, initiation, routine, and close-out) for oncology clinical trials in accordance with study protocols and regulatory requirements.
- Assist in site selection and feasibility assessments.
- Ensure proper documentation and timely resolution of site issues.
- Support site staff in understanding and complying with study protocols and GCP guidelines.
- Verify source data and case report forms (CRFs) for accuracy, completeness, and consistency.
- Ensure timely collection and review of essential regulatory documents.
- Track patient recruitment and retention efforts at assigned sites.
- Participate in CRA training sessions, project team meetings, and sponsor meetings as required.
- Maintain high-quality communication with clinical sites and sponsor/CRO teams.
- Escalate site performance or compliance issues as needed.
Required Qualifications
- Bachelor’s degree or higher in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 1–2 years of clinical research experience (internships or study coordinator experience may be considered).
- Exposure to oncology trials (academic, site, or CRO experience).
- Understanding of ICH-GCP guidelines and regulatory requirements.
- Strong organizational skills with attention to detail.
- Ability to manage multiple tasks and priorities independently.
- Excellent communication and interpersonal skills.
- Proficiency with clinical trial management systems (CTMS), EDC systems, and Microsoft Office.
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