Freelance Study Start-Up and Regulatory Specialist

4 days left

Salary: On application
05 Feb 2021
07 Mar 2021
Regulatory Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)

I’m currently partnered with a Global CRO that’s looking for a Freelance Study Start-Up and Regulatory Specialist based in Netherlands on a 9 month contract for a full FTE.



  • Performs assigned activities across Netherlands in all phases of clinical trials
  • Provide delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, as well as review and finalise essential documents required for site initiation
  • Develops plans in accordance with Standard Operating Procedures as well as complying with all controlled documentation requirements to ensure quality results
  • Accountable for negotiations and executions of clinical trial agreements and budgets
  • Ensure all relevant documents are submitted to the Trial Master File (TMF) as per company SOPs



  • Background in regulatory submissions across Netherlands
  • Excellent verbal, interpersonal, and written communication skills in Dutch and English
  • Strong knowledge of clinical trials
  • BA/BS degree in the science/health care field
  • Ability to successfully support internal and external customers


To discuss this role in further detail, please get in touch on +44 1273 952187 for more information.


Salary: On application

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