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 joinusaccessiontherapeutics.com 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