At a Glance
- Tasks: Monitor clinical trial sites and ensure compliance with regulations while supporting innovative medical research.
- Company: Join IQVIA, a top-rated workplace recognised for its commitment to innovation and employee satisfaction.
- Benefits: Enjoy competitive pay, flexible travel opportunities, and a chance to make a real impact in healthcare.
- Other info: Dynamic role with opportunities for growth in a leading global clinical research company.
- Why this job: Be part of a mission to improve patient outcomes and work on groundbreaking medical treatments.
- Qualifications: Experience in clinical monitoring and knowledge of GCP and ICH guidelines required.
The predicted salary is between 35000 - 45000 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s Site Management (multi-sponsor) team is growing and seeking experienced Clinical Research Associates. We are recognised as a 2026 "Glassdoor Best Place to Work in the UK" and #1 in our category on the 2026 Fortune® World’s Most Admired Companies™ list.
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 Harmonisation (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
- Experience of independent on‑site monitoring.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites.
About IQVIA
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.
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. Please note - this role is not eligible for UK visa sponsorship.
CRA II, Oncology Manchester employer: Meeveem Limited
At IQVIA, we pride ourselves on being a top employer, recognised as a 2026 'Glassdoor Best Place to Work in the UK' and #1 in our category on the Fortune® World’s Most Admired Companies™ list. Our Manchester location offers a collaborative work culture that fosters professional growth through continuous training and development opportunities, ensuring that our Clinical Research Associates are well-equipped to make a meaningful impact in the field of oncology. Join us to be part of a mission-driven team dedicated to accelerating innovation for a healthier world.
StudySmarter Expert Advice🤫
We think this is how you could land CRA II, Oncology Manchester
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We think you need these skills to ace CRA II, Oncology Manchester
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meeveem Limited!
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How to prepare for a job interview at Meeveem Limited
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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