We are working in partnership with a unique small Life Science service provider with a core focus in clinical pharmacology and Oncology that are looking for an Associate Medical Director to join their clinical pharmacology unit.
Due to their niche focus, my client have built an excellent market reputation for being specialists in their area and as a result have been growing significantly over the last 2-3 years across their global teams, making it a great time to join them on this journey an a unique environment to develop you career.
Responsibilities include:
- Ensure safety and welfare of trail participants and deliver of high quality studies in the clinical pharmacology unit
- Perform screening, ongoing monitoring and post-study clinical examinations
- Perform the role of the Principal Investigator (including First-In-Human) for clinical trials
- Line management of a small team of Research Physicians and provide support and guidance to the Head of Departments for the clinical and enrolment departments.
- Deputise the Senior Medical Director
- Participate in commercial development activities including feasibility assessments and budget reviews when required
- Assess and develop key trial documents and reports including study protocols, risk management plans and safety reports
- Evaluate participants eligibility and obtain written consent for inclusion in studies
Requirements
- Medical degree with GMC registration
- Experience conducting clinical trials in a clinical pharmacology unit
- Experience as the Principal Investigator in First-In-Human studies
- Strong knowledge and understanding of MHRA Phase I accreditation requirements
- Previous line management experience
Benefits
- Hybrid Working
- Car allowance
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Last updated on Jun 13, 2024