Senior Clinical Research Associate (UK Based) (Freelance)
I’m partnering with a great client who cover most of the EU/UK. My client supports clinical studies across all therapeutic areas, and they have supported the trials of most of todays top selling drugs.
You will be an influential member of the wider team.
You will be responsible for site management, monitoring and close out of assigned clinical trials investigator sites to ensure safety for our patients and quality study execution.
SPECIFICS ABOUT THE ROLE
- Ensure proper conduct of clinical trials in accordance with Study Monitoring Plan.
- Serve as a point of contact for audit conduct and drive audit observation CAPA* development and check.
- Interface with the study team as needed, create information flow between members of the study team, vendors and assigned investigator sites.
IS THIS YOU?
We are looking for a professional who has the determination and courage always to put patient well-being first.
REQUIREMENTS
- Bachelor’s degree in life science or professional degree in life science.
- Monitoring experience: Minimum 3.5 years of relevant experience in clinical research site monitoring (preferably in Oncology)
- Extensive knowledge of clinical trial methodologies.
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases.
Senior Clinical Research Associate (Freelance) employer: Barrington James Limited
Join a well-established organisation that values its employees and fosters a supportive work culture. As an HR Associate, you will have the opportunity to be a trusted point of contact, ensuring compliance with employment legislation while contributing to the development of robust people processes. With a focus on employee growth and continuous improvement, this role offers a meaningful career path in a dynamic environment.
