Clinical Study Manager

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: ·       Daily interaction and collaboration with CROs and third-party vendors delivering the clinical trials; ·       Liaising with study sites to support clinical trial delivery, efficiency and data integrity; ·       Maintenance and management of clinical trial documentation; ·       Tracking site performance, equipment, budgets and sample management; ·       Providing additional support,  as required.
CANDIDATE WILL NEED:  ·       Good educational background; at least 4-5 years' experience working in a relevant role; ·       Good communication skills; ·       Willingness to make occasional study site visits, as required; ·       Ability to work effectively in cross-functional teams; ·       Understanding  of the requirements of relevant regulatory and healthcare bodies; ·       Willingness to undertake additional activities to support other departments; ·       Experience of or interest in Data Management or Pharmacovigilance (desirable); ·       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  ******                                               Any personal data that is sent in connection with applications will be used by us in accordance with our privacy policy https://www.accessiontherapeutics.com/recruitment-privacy-policy