Clinical Research Associate II

IQVIA Inc; Bath; Remote; GBP 40,000 - 65,000; Full time

Job summary

IQVIA is seeking a Senior Clinical Research Associate to join our Clinical Functional Service Partnerships in the United Kingdom. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring patient safety and data integrity while supporting study timelines and cross-functional teams.

This on-site role requires 2+ years of monitoring experience, strong GCP/ICH knowledge, and the ability to travel up to 60% within the region.

Qualifications

• University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience.
• 2 years minimum on-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment.
• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
• Preferrable experience in a sponsor-dedicated or cFSP environment.
• Knowledge of patient recruitment and study start-up activities is preferred.
• Excellent communication, organizational, and stakeholder management skills.
• Ability to work independently, manage multiple priorities, and collaborate effectively within cross-functional teams.
• Willingness to travel within the assigned region (up to 40-60% of working time).

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits following protocol, GCP, ICH guidelines, and regulatory requirements.
• Ensure sites maintain high standards of patient safety, data integrity, protocol compliance, and study quality.
• Build and maintain relationships with investigators and site personnel, providing guidance, training, and support.
• Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution, and site performance metrics.
• Collaborate with sites to implement patient recruitment and retention strategies to meet timelines.
• Maintain inspection-ready study documentation (ISF, TMF, monitoring reports, follow-up communications).
• Identify, assess, and elevate study risks, site issues, and quality concerns with timely resolution.
• Partner with cross-functional study teams to support successful study execution and delivery of project objectives.
• Mentor and support junior clinical team members through coaching, training, and co-monitoring activities.
• Contribute to continuous improvement initiatives and support study start-up, maintenance, close-out, and site financial activities as required.

Skills

GCP/ICH knowledge

Communication

Independent work

Travel willingness

Patient recruitment

Study start-up

Cross-functional collaboration

Stakeholder management

Education

Life Sciences / Health Sciences degree

Job description

Why Join Clinical Functional Service Partnerships (CFSP)?

At IQVIA, our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA. You’ll develop deep, specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses - and the security of a long-term IQVIA career even as individual programs evolve.

Through our long-standing partnerships with the world’s leading pharmaceutical and biotechnology companies, you’ll contribute to clinical research programs that bring innovative treatments to patients worldwide, working across all phases of development and a broad range of therapeutic areas, within a culture that supports flexibility, continuous learning, and wellbeing.

Key responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols, GCP, ICH guidelines, and applicable regulatory requirements.

• Ensure investigational sites maintain high standards of patient safety, data integrity, protocol compliance, and study quality.

• Build and maintain effective relationships with investigators and site personnel, providing ongoing guidance, training, and support throughout the study lifecycle.

• Monitor study progress, including regulatory documentation, patient recruitment and enrollment, data query resolution, and site performance metrics.

• Collaborate with sites to implement and optimize patient recruitment and retention strategies to support study timelines.

• Maintain accurate, complete, and inspection-ready study documentation, including Investigator Site Files (ISF), Trial Master Files (TMF), monitoring reports, and follow-up communications.

• Identify, assess, and appropriately elevate study risks, site issues, and quality concerns while driving timely resolution.

• Partner closely with cross-functional study teams to support successful study execution and delivery of project objectives.

• Mentor and support junior clinical team members through coaching, training, and co-monitoring activities, as applicable.

• Contribute to continuous improvement initiatives and support study start-up, maintenance, close-out, and site financial activities as required.

What you’ll bring

• University degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline, or equivalent combination of education and experience.

• 2 years minimumon-site monitoring experience of clinical trials within a CRO, pharmaceutical, biotechnology, or healthcare environment.

• Strong knowledge of GCP, ICH guidelines, and applicable regulatory requirements.

• Preferrable experience in a sponsor-dedicated or cFSP environment.

• Knowledge of patient recruitment and study start-up activities is preferred.

• Excellent communication, organizational, and stakeholder management skills.

• Ability to work independently, manage multiple priorities, and collaborate effectively within cross-functional teams.

• Willingness to travel within the assigned region (up to 40-60% of working time).

Please note this position cannot offer visa sponsorship, candidates must hold right to work in UK & Ireland.

Build Your Future with IQVIA

As a Senior CRA at IQVIA, you’ll apply your clinical research expertise to drive meaningful outcomes for patients and sponsors around the world. You’ll work on innovative studies across a variety of therapeutic areas, collaborate with industry-leading professionals, and take on increasingly strategic responsibilities throughout the clinical trial lifecycle. With continuous professional development, global career opportunities, and a culture that values expertise and innovation, IQVIA provides the platform to elevate your career and make a lasting impact on healthcare.

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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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.