Global Medical Director - Neurology/ Rare Disease

Location
Belgium (BE)
Salary
Competitive
Posted
23 Feb 2021
Closes
25 Mar 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Senior Management

We are seeking an experienced physician within phase I-III clinical development to work on innovative molecules for an exciting biotech company, with a focus on novel treatments in the neurology/ rare disease therapeutic area. 

The Role(s):

The role is responsible for input and oversight for early / late stage clinical development plans within the department. The successful applicant(s) will be responsible for leading the development of key products in these areas. The main purpose of the role will be to oversee a series of trials, draft study specific documentation such as NDA / CTA submissions and Investigator Brochures, alongside reviewing study data and providing expert advice to aid in the development of the disease portfolio.

Further Key Responsibilities:

  • Directing and overseeing clinical research plans, and providing input to help integrate the Clinical Development Plan with the Drug Development Plan
  • Provide strategic oversight on pipeline progression
  • Serving as the clinical / medical team expert to provide direction to all project team functions, regularly liaising with KOL's and organizing Advisory Board Meetings
  • Implementing strategies to identify, monitor and resolve clinical / program trial issues
  • Reviewing / monitoring safety study data and providing clinical expertise and content to regulatory documents
  • Proactively and independently find solutions and drive innovation

Your Background:

  • Educated to Medical Degree
  • Board Certification / specialist training required (Neurologist)
  • Demonstrable experience in Phase I-III clinical trial management
  • Investigator experience
  • Ability to influence others; self-starter with an inquisitive nature and practical approach to problem solving
  • Demonstrated competence as Study Director / Medical Monitor / Research Physician / Medical Advisor and prior experience working with the FDA or EMEA on responses to inquiries for study related in

Benefits:

  • Comprehensive salary
  • Enhanced bonus scheme
  • Long term incentives
  • Travel allowance
  • 30+ days holiday
  • Clear development pathway

If you are interested, get in touch with me ASAP…

Vincenzo Dessena – Barrington James – Associate Consultant

Vdessena (at) barringtonjames.com

 

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