• MAC - FULL TIME

MEDICAL DIRECTOR

Closing date for applications: 31 May 2022

MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.


We are seeking to appoint a Medical Director to join our team and make a positive impact in a growing and progressive CRO. You will be joining a company that put the needs and wellbeing of their people first, who are inclusive and who deliver exceptional service – together.


The role is full time and home based (UK or EU) with business related travel as required”.


The focus of the job is to provide medical management and professional medical support for clinical research projects at MAC CRO services as the assigned Medical Monitor. To act as main point of medical contact in activities such as training of investigator sites and the study team, review and design of study protocols, assistance with feasibility and proposals and business development.


KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:

  • MD degree as a Doctor/Physician with License to practise in the base country

  • A minimum of 2 years of experience of medical monitoring in industry or CRO setting – Essential

  • Additional post graduate degree in Internal Medicine, Psychiatry or equivalent- Preferred

  • Diploma of Pharmaceutical Medicine – Preferred

  • Clinical Pharmacology degree / knowledge- Preferred

  • Home based in the UK or Europe

  • Willing to travel to US

RESPONSIBILITIES:

  • Acts as Medical Monitor for the clinical studies they are assigned as MM

  • Drafts and approves the study specific Medical Monitoring plans

  • Main point of contact for protocol specific and medical concerning including but not limited to subject eligibility, evaluation and reporting of adverse events (AEs) and follow up

  • Reviews study data on ongoing basis

  • Acts as member of Safety Review Committees and Dose Review Meetings as required

  • Collaborates with MAC PV team to process Serious Adverse Events (SAEs)

  • Contributes medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc.

  • Provides after hours medical support for projects assigned

  • Provides therapeutic and protocol-specific training to the project teams

  • As directed supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management

  • Collaborates with Medical Writing and Sponsors in reviewing and/or assisting in the preparation of final study reports (CSRs), or other study documentation (Protocols, IBs, SRC charter, MMPs etc.,)


Job Description - Medical Director
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Salary: Competitive + Negotiable £ Apply Now

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