516 Iqvia jobs in the United Kingdom

**Join us on our exciting journey!**
IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward. Our solutions are powered by the IQVIA CORE, which combines big data, advanced technology, analytics, and extensive industry knowledge. IQVIA has approximately 90,000 employees worldwide.
IQVIA helps clients to improve their clinical, scientific, and commercial results and seamlessly connects clinical and commercial execution to real-world outcomes. This allows its clients to realise the full potential of their innovations. From pipeline to portfolio to population health, IQVIA aims to be a transformational partner to its healthcare clients globally. Critically, IQVIA today sells both to R&D and Commercial stakeholders, from the C-Suite down. The company has a strong balance sheet and remains highly acquisitive.
**Director, Business Development - IQVIA Biotech**
**The Role**
IQVIA is currently looking to appoint a driven and experienced BD professional, to work specifically within the domain of Biotech, providing customized Phase I through IV services globally, and offering expertise across multiple therapeutic areas. The individuals will be based anywhere in Europe.
This is a critical appointment as part of a company-wide initiative, who are not only focussed on increasing our client portfolio through successful sales and business development, but who will develop trusted relationships which will enable IQVIA to sell across the enterprise/continuum over time.
IQVIA envisions significant additional clinical upside in a market that remains well-positioned for further consolidation. The key will be effectively harnessing its integrated solutions portfolio in such a way as to move beyond transactional, reactive sales activity to shape understanding around the IQVIA expanded platform. Inevitably, this will necessitate positioning the end to end offering discussions to a higher level with existing and future clients.
The EBP sales specialist will be responsible for selling the entire solution portfolio across Clinical, thereby fulfilling every client need across the product lifecycle. These individuals will need the seniority and gravitas to engage credibly at C-Suite level with Biotech clients, navigating internally across the account and pulling together the optimal IQVIA expert teams as required. They will gather the required internal, external, and competitive intelligence on their clients, develop a robust, systematic account strategy and drive superior execution to identify, drive and expand the business across the entire IQVIA clinical solution portfolio.
Critically, these individuals will be required to sell and close the bigger value deals and so IQVIA needs to appoint strategic sales and business development leaders with the experience and gravitas to operate at this level. Candidates will need to bring past solution selling expertise with a track record of leveraging organizational capabilities to upsell, driving a more sophisticated and integrated sales approach helping to shift the market to the benefit of the company.
**The person**
In terms of the preferred profile for a Biotech specialist, they should possess strong intellect and analytical acuity and with the ability to define, conceptualise and, ultimately, sell, the company's integrated clinical solution portfolio. The individual will need to display strong 'hunting' skills, to engage and open out new relationships, as well as broadening the opportunity within the existing client base.
The individual will be required to work collaboratively across the organization; a sophisticated approach to relationship building, both internal and external, will also be essential.
Certainly, the company needs to appoint individuals who can hit the ground running and, consequently, an established network within the markets of relevance would be advantageous.
The appropriate drive and resilience will be reflected in a track record of R&D/Clinical and business development contribution in past roles.
**Skills**
+ 10 years of related experience in a CRO, pharmaceutical or biotechnology environment.
+ At least 10 years' experience as a BD Director in a CRO environment.
+ Understanding of the clinical process (PH I - IV).
+ Solid understanding of commercialization and the principles of drug discovery and development.
+ Have a detailed understanding of the Biotech Market place
**Moving healthcare forward. Together.**
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
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

**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, 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

**Job Title: Remote Gastroenterologist Consultant - UK Registered | IQVIA Healthcare Professionals Network**
**Location** : Remote (UK-based)
**Contract Type** : Freelance / Part-time / Flexible
Are you a GMC-registered Gastroenterologist seeking flexible, remote opportunities? Join the IQVIA Healthcare Professionals Network and help shape the future of virtual care from the comfort of your home.
We are looking for experienced UK-registered gastroenterologists to conduct remote patient assessments. You'll contribute to patient monitoring, and innovative healthcare initiatives.
**Responsibilities**
+ Conduct remote gastroenterology assessments via secure digital platforms
+ Review patient histories, test results, and clinical data
+ Provide expert clinical opinions and documentation
+ Collaborate with multidisciplinary teams across the UK and Europe
+ Ensure compliance with clinical governance and data protection standards
**Requirements**
+ UK registered with a license to practice in the UK
+ Must be based in the UK
+ Proven experience in gastroenterology (NHS or private sector)
+ Comfortable using digital tools for patient interaction
+ Excellent written and verbal communication skills
+ Reliable internet connection and secure working environment
#LI-CES
#LI-CT1
#LI-HCPN
#LI-DNP
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

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

_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 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.
+ Permanent right to Work in the UK is required.
**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

Clinical Research Associate (CRA) – Hybrid – London Region RBW Consulting is excited to announce an opportunity on behalf of a small CRO client we are partnered with. This company focuses on UK-based studies and site visits are regionally based around the London area. This opportunity offers exposure to varied therapy areas, manageable site visits, and the chance to develop beyond traditional monitoring responsibilities. The Role You’ll be working on a broad portfolio of studies, from initiation through to close out, across multiple therapy areas including respiratory and emerging fields. This hybrid position involves monitoring sites (primarily in and around London) and attending the office approximately twice per month. Key responsibilities include: Monitoring visits at UK trial sites Setting up, managing, and maintaining eTMFs Ensuring delivery of studies within budget and timelines Liaising with sponsors, vendors, and internal teams to maintain project oversight Supporting colleagues through training and mentoring in areas of expertise Contributing to project, client, and team meetings What We’re Looking For At least 1 year experience as a CRA (can consider candidates with academic or industry experience) A proactive approach with the flexibility to handle multiple priorities in a dynamic environment The Offer Salary range: £40,000–£47,000 , with potential annual increases 25 days annual leave plus standard benefits Hybrid working model (office attendance twice per month) Opportunities for professional growth, with development into Senior CRA or Project Management roles This role is ideal for CRAs who enjoy a mix of independence and collaboration, and who want to be part of an organisation that values quality, career growth, and work-life balance. To apply: Please click ‘apply’ or contact Joe Pearce for any further information About RBW Consulting RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain. We are an equal opportunities Recruitment Business and Agency RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

Clinical Research Associate (CRA) – Hybrid – London Region RBW Consulting is excited to announce an opportunity on behalf of a small CRO client we are partnered with. This company focuses on UK-based studies and site visits are regionally based around the London area. This opportunity offers exposure to varied therapy areas, manageable site visits, and the chance to develop beyond traditional monitoring responsibilities. The Role You’ll be working on a broad portfolio of studies, from initiation through to close out, across multiple therapy areas including respiratory and emerging fields. This hybrid position involves monitoring sites (primarily in and around London) and attending the office approximately twice per month. Key responsibilities include: Monitoring visits at UK trial sites Setting up, managing, and maintaining eTMFs Ensuring delivery of studies within budget and timelines Liaising with sponsors, vendors, and internal teams to maintain project oversight Supporting colleagues through training and mentoring in areas of expertise Contributing to project, client, and team meetings What We’re Looking For At least 1 year experience as a CRA (can consider candidates with academic or industry experience) A proactive approach with the flexibility to handle multiple priorities in a dynamic environment The Offer Salary range: £40,000–£47,000 , with potential annual increases 25 days annual leave plus standard benefits Hybrid working model (office attendance twice per month) Opportunities for professional growth, with development into Senior CRA or Project Management roles This role is ideal for CRAs who enjoy a mix of independence and collaboration, and who want to be part of an organisation that values quality, career growth, and work-life balance. To apply: Please click ‘apply’ or contact Joe Pearce for any further information About RBW Consulting RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain. We are an equal opportunities Recruitment Business and Agency RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

This is an exciting opportunity for a Sub-Investigator/ Clinical Research Physician to join an innovative medical company 2 days a week (up for discussion). WHY CONSIDER THIS ROLE & COMPANY? Working for an established and recognised global leader in their chosen therapeutic area Company going through a consistent period of growth (including internationally) with multiple clinics across the UK You’ll work for a company who value the ongoing training and development of their team with hard working and proactive team players consistently seeing opportunities for career growth KEY RESPONSIBILITIES: Responsible for supervising the trial site and delegating all tasks associated with it Oversee all team members and ensure they perform their duties according to set protocols Ensure that access to all tools compatible with what is required in the study protocol is accessible to everyone Follow specific regulations whilst conducting the studies Ensure all medical records/study documentation is accurate REQUIREMENTS: You will be a Medical Doctor with clinical research experience and be GMC registered You will, preferably, have MRCP or similar membership exams Exposure in clinical research phases 0 to 4 would be highly desirable Great management and leadership skills Fast paced and dynamic individual 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.