Clinical Study Manager

Hobson Prior are currently recruiting for a Clinical Study Manager to join rapidly growing biotechnology company where you will become a part of their clinical research team. You will be accountable to supervise clinical studies and help the organisation become a worldwide forerunner for modern immunotherapies against cancer.

Job Responsibilities:

• Assurance of upholding project timelines, quality standards and study objectives.
• Planning and conduct of training sessions relevant to the studies as well as team and investigator meetings.
• Preparation and clearance of study documents with CROs as well as the selection of contract partners.
• Compilation of documents for the authorization of clinical studies, for ethics commissions and for federal authorities.
• Preparation of study information according to regulatory requirements.

Key Skills:

• Proactive, independent way of working as well as excellent communication and organization skills.

Requirements:

• Degree in natural sciences or completed medical vocational training.
• Professional experience as a Clinical Study Manager, CRA/Clinical Monitor (m/f) or in a similar function.
• Profound knowledge in the field of oncological studies. Very good knowledge of relevant laws and regulations (e.g. ICH GCP guideline).
• Professional handling of MS Office.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.