Accessibility Links

Medical Monitor DACH - Medical Director Level

  • Job type: Permanent
  • Location: Munich
  • Job reference: RATR2407201703
  • Sector: Clinical Development, Clinical, EPM Scientific
  • Date posted: 24/07/2017
The Medical Monitor will be responsible for medical affairs activities covering the DACH Region. 
Will be overseeing scientific exchange between healthcare professionals and KOLs within the Oncology Space as well as oversee the development arm.  

This is a Director Level opportunity and is with an upcoming Biotech, Our clients are looking for someone with both Medical Affairs and Clinical Development experience to oversee the entire pipeline. 

Key Responsibilities include:
  • Engaging and expanding local and national KOL Network within Oncology and maintaining strong scientific Relationships with them.
  • Will be the main point of contact for investigators that seek to develop a relationship with the company's commercially available assays in oncology.
  • Develop and implement strategy across Europe and key countries of operation. 
  • Lead advisory boards to seek external advice.
  • Act as the main point of contact for the scientific and academic community and deal and answer scientific questions.
  • Take active part and support during international and regional medical congresses.
  • Supporting Training, for both Medical and Commercial 
  • Accountability for safety across the study.
  • Provide medical expertise to the study team during key activities.
  • Review study level data.
  • Address safety issues across the study.
  • Coordinate, review and approve the key documents such as protocol and clinical study report.
  • Play a key role in the interaction with regulatory authorities.
  • Identify opportunities to create a project publication plan when required.

Skills Required:
  • Engaging and expanding local and national KOL Network within Oncology and maintaining strong scientific Relationships with them.
  • Industry experience in Oncology with a proven track of contribution to commercial, medical and or clinical development strategies. 
  • Expert at life-cycle management strategy and execution.
  • Previous Managerial Experience
  • Education minimum Requirement:           MD, PharmD or equivalent
  • Excellent presentation and teaching skills
  • Effective oral and written communication skill
  • Fluent in English and German


CV’s reviewed immediately

Only candidates that fill the full requirements will be contacted

Similar jobs
Regulatory Affairs Specialist
  • Job type: Permanent
  • Location: Cologne
  • Salary: Competitive
  • Description Regulatory Affairs Manager An innovative medical device manufacturer is seeking a Regulatory Affairs Specialist, required for in Cologne, Germany. The Regulatory Affairs
Sr. Supervisor, Production Manufacturing - Medical Device
  • Job type: Permanent
  • Location: Miami
  • Salary: Competitive
  • Description SENIOR SUPERVISOR, PRODUCTION (MANUFACTURING) Medical Device Company - Thoracic & Aortic AreasMiami, FL$80,000
Medical Director - Neurology
  • Job type: Permanent
  • Location: Chicago
  • Salary: $230000 - $250000 per annum
  • Description The Medical Director, Neurology will serve as the internal medical and scientific expert for assigned neurology product(s), driving key medical strategies and tactics which align...
Senior Clinical Quality Manager
  • Job type: Permanent
  • Location: Zürich
  • Salary: Competitive
  • Description Description: A highly-innovative Start-Up company specialising in Oncology is seeking a Senior Clinical Quality Manager based
Sr. Medical Director, Medical Affairs
  • Job type: Permanent
  • Location: New Jersey
  • Salary: $250000 - $290000 per annum
  • Description The Medical Director, Medical Affairs will be responsible for working with key stakeholders to develop and execute the medical affairs plans for pipeline assets in...