Accession Therapeutics Limited, a vibrant, early-phase biotechnology company based in Oxford, is looking for a Clinical Study Manager to assist with the set-up, management, and delivery of the company’s clinical trials in compliance with study protocols and GCP and regulatory standards.
You will join a small Clinical Operations team, working closely with the Medical Director, Quality, CMC, and Translational Medicine teams; activities will be commensurate with experience.
RESPONSIBILITIES TO INCLUDE:
1. Daily interaction and collaboration with CROs and third-party vendors delivering the clinical trials;
2. Liaising with study sites to support clinical trial delivery, efficiency, and data integrity;
3. Maintenance and management of clinical trial documentation;
4. Tracking site performance, equipment, budgets, and sample management;
5. Providing additional support, as required.
CANDIDATE WILL NEED:
1. Good educational background; at least 4-5 years’ experience working in a relevant role;
2. Willingness to make occasional study site visits, as required;
3. Ability to work effectively in cross-functional teams;
4. Understanding of the requirements of relevant regulatory and healthcare bodies;
5. Willingness to undertake additional activities to support other departments;
6. Experience of or interest in Data Management or Pharmacovigilance (desirable);
7. Experience of early-phase oncology and ATMP (desirable).
Accession offers a good salary and company benefits including pension, private health insurance, life insurance, and subsidised local gym membership.
To apply for this position please send a LETTER OF APPLICATION (essential) and a COPY of your C.V. to joinus@accessiontherapeutics.com
Any personal data that is sent in connection with applications will be used by us in accordance with our privacy policy here.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Biotechnology
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