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Trial Manager

Locatie

Oss

Contactpersoon

Susan van den Bulk People in Science
M: (06) 2300 4468 
E: s.vdbulk@peopleinscience.nl 

Profile of the Trial Manager

  • Life Science Master’s Degree prefered
  • A minimum of three years experience in project management of clinical trials.
  • Effective communication in English (oral and written)
  • Demonstrated good teamworker
  • 80-100% employment

Functie-omschrijving van de Trial Manager

Global Trial Management (GTM) is an organization accountable for all HQ sponsored clinical trials (Phase II-V). GTM is based in the US and Oss. The GTM Trial Manager will lead the Clinical Trial Team (CTT) and will be assisted by the GTM Trial Specialist (TS).

  • Accountable for the operational planning and execution of Clinical Trials from planning through Clinical Study Report
  • Leads the Clinical Trial Team (CTT)
  • Manages and oversees the completion of country feasibility, protocol feasibility and investigator meetings
  • Facilitates the development of protocol level budgets and obtains budget approval including management of the triallevel budget
  • Participates in Vendor selection and acts as primary contact with vendors.
  • May manage direct reports

Bedrijfsprofiel

MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies, and consumer and animal products, we work with customers and operate in more than 140 countries to deliver innovative health solutions. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD is the name of Merck outside the US and Canada. MSD has a workforce of over 6.000 in the Netherlands at five different
sites. MSD is the largest pharmaceutical company in the Netherlands. It has large production facilities for Human Health and Animal Health in Oss, Haarlem and Boxmeer and R&D facilities in Boxmeer and Oss. The MSD Development Center in Oss (DCO) supports MSD’s need for product development activities, particularly for the emerging markets. The DCO is also involved in Product Value Enhancement and it supports MSD’s early phase clinical research in multiple therapeutic areas.