Senior Clinical Research Associate, Oncology in Manchester

Senior Clinical Research Associate, Oncology in Manchester

Manchester Full-Time No working from home possible
IQVIA Argentina

Senior Clinical Research Associate, Oncology

Manchester, United Kingdom | Full time | Field-based | R1516890

Join IQVIA on our mission to accelerate innovation for a healthier world!

IQVIA’s Site Management (full service / multi-sponsor) team is growing and seeking Senior Clinical Research Associates in the UK.

Why IQVIA?

  • Genuine career development opportunities to grow as we grow
  • AI‑powered career advancement through our internal talent marketplace, Career Connections
  • Mentorship opportunities across the organisation via Employee Resource Groups
  • Flexible working to assist work–life balance and professional success
  • Well‑being support covering your physical, mental, and financial health

Awards

  • 2026 "Glassdoor Best Place to Work in the UK"
  • #1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)
  • Brandon Hall Excellence Award for Learning & Development

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) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP 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

Requirements

  • Requires at least 3-5 years on-site monitoring experience of interventional studies
  • Degree in scientific discipline / health care or equivalent industry experience
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Ability to establish and maintain effective working relationships with coworkers and clients
  • Full driving license and access to vehicle for travel to sites

Please note - this position is not eligible for visa sponsorship

#LI-ADAMTHOMPSON

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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

"I like that we're different. I like that we're a unique organization unlike any other. I like to think of us as the intelligence company for life sciences and healthcare. I do believe there's nothing else like this organization in the world. So if you like something that's different and interesting, you're going to like IQVIA. If you like an organization that has a variety of opportunities, from IT to big data to AI to finance to HR, there are so many opportunities to have an impact."

"The culture in IQVIA is to be constantly looking at how we can do things better to help our customers, to bring life-changing medicines to patients and also to be a part in designing and developing and implementing these solutions. And so I think it's a great place to join because there is that organizational focus and commitment in driving forward the innovation and just the ability, I think, to work with cross-functional teams who are all excited to be working in these areas. It's a fantastic opportunity."

"First of all, we are humans, we have some moments in our lives that are so very important and we need to respect. And something I also always love about IQVIA was that my leaders and people with which I have been working, they always respected a lot as well our personal lives. I never miss a parents' meeting of my kids, and this is something that we shouldn't be giving for granted."

Senior Director Global Site Activation

"I like that we're different. I like that we're a unique organization unlike any other. I like to think of us as the intelligence company for life sciences and healthcare. I do believe there's nothing else like this organization in the world. So if you like something that's different and interesting, you're going to like IQVIA. If you like an organization that has a variety of opportunities, from IT to big data to AI to finance to HR, there are so many opportunities to have an impact."

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Senior Clinical Research Associate, Oncology

Manchester, United Kingdom | Field-based

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Senior Clinical Research Associate, Oncology in Manchester employer: IQVIA Argentina

At IQVIA, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our Reading location offers a hybrid working model, allowing for flexibility while engaging in meaningful projects that impact clinical outcomes globally. We are committed to employee growth, providing ample opportunities for professional development and mentorship, making it an ideal place for those looking to advance their careers in clinical research.

IQVIA Argentina

Contact Details:

IQVIA Argentina Recruitment Team