Job Title: Senior CRA
Location: Home-based with travel required
Employment Type: Full-time/Permanent
Our client, a global leader in clinical research, is seeking a driven Senior Clinical Research Associate (CRA) to join their team. This is your chance to work at the forefront of science, partnering on multi-sponsor studies that span biotech and pharma, with a strong emphasis on innovative therapeutic areas such as rare disease, oncology, and cell & gene therapy.
What You’ll Do:
* Lead independent on-site monitoring of clinical trial sites, ensuring data quality and patient safety at every step.
* Conduct initiation, monitoring, and close-out visits, delivering clear, insightful reports.
* Ensure all study activities comply with ICH-GCP, SOPs, and study protocols.
* Review documentation for accuracy, completeness, and compliance.
* Collaborate with investigators, site staff, and cross-functional teams to drive performance and troubleshoot study challenges.
What We’re Looking For:
* Bachelor’s degree or higher in health, medical, or life sciences (veterinary science not accepted).
* 2+ years of independent clinical monitoring experience in a CRO or sponsor environment.
* Strong knowledge of ICH-GCP guidelines and clinical trial processes.
* Excellent communication and problem-solving skills; ability to work independently and collaboratively.
* Willingness to travel regularly to investigator sites.
* Desired: Previous monitoring experience in oncology or other complex therapeutic areas.
Apply Now
Take the next step in your career and lead where it matters most.
Please note: If you are interested in finding out more about this role or others, please contact Jada Kirlew at jkirlew@i-pharmconsulting.com or call: +44 (0)20 7551 0727