Medical Director

Location
Homeworking
Salary
Competitive
Posted
13 May 2021
Closes
11 Jun 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Senior Management

I am currently partnered with an exciting medical technology company, looking for the expansion of their global clinical development team. My client is a world-leading innovator with around 50,000 employees globally.

Focusing on the clinical development of immune-oncology and oncology products, you will be responsible for the design and execution of the clinical development portfolio, ranging from pre-clinical, regulatory and commercial stages of the various products.

If you are a physician with industry experience in oncology, immune-oncology, radiology or nuclear medicine, please read further:

Responsibilities:

  • Lead the clinical development in cross functional projects and products within internal and external teams (Including RA, QA, radiochemistry, product management, academic and CRO partners)
  • Responsible for the implementation and development of the medical strategy of the portfolio
  • Responsible for the quality and timely completion of all project documentation including; case study reports, protocols, and protocol amendments
  • Work with cross functional teams to minimize risk and uphold and ensure patients safety at all times
  • Working with internal and external teams to create clinical development plans and support actions within regulatory approval, adoption and reimbursement
  • Develop and maintain external networks of key leaders and providing medical insight to new and evolving opportunities within oncology and immune-oncology
  • Compliance with in house quality management, systems, policies, goals and applicable laws and regulations designated to the role
  • Work with other members on scientific publications in refereed journals 

Experience:

  • Medical degreeSpecialisation or board certification in Radiology, nuclear medicine, on oncology or equivalent
  • Experience in the industry as a medical director or equivalent in the pharma, CRO or biotech environment
  • Experience in clinical trials from an industry perspective, with record or phase 1-4 study management 
  • Strong level of English and eligibility to work in the EU 

Desirable

  • Experience in translational pre-clinical clinical trials and/or study concepts
  • Experience of program level strategy support
  • Experience in molecular imagery or similar
  • Experience working on scientific publications as an author or co-author

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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