Proclinical is seeking a dedicated individual for the role of Associate Director, Clinical Data Management. The successful candidate will be responsible for leading the team and overseeing the execution of clinical trials.
Responsibilities:
- Organise and conduct team meetings.
- Foster team development and identify high-performance team members.
- Collaborate with the (Senior) Director Clinical Data Management on team development.
- Provide guidance to project teams on the oversight and supervision of CRO/third party vendors and organize trainings as needed.
- Act as a mentor for new team members.
- Contribute to the development and review of portfolio documents (includes contracts, guidelines, budgets, metrics, KPIs).
- Ensure compliance with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.
Key Skills and Requirements:
- Extensive knowledge of Clinical Data Management with a focus on DM activities as a Lead and DM project management.
- In-depth knowledge of international guidelines (ICH-GCP) for the conduct of clinical research projects.
- Experience with Clinical Database Systems and processes.
- Proven experience in resource planning.
- A background in natural/life sciences or relevant experience in a CRO/ biotechnology/ pharmaceutical company in a Clinical Data Management position.
Interested or know someone who might be? Reach out to Heidi Hennigan using the following:
✉️ h.hennigan@proclinical.com
📞 020 38541033
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.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. is acting as an Employment Agency in relation to this vacancy.
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