Freelance Study Start-Up and Regulatory Specialist

Location Netherlands
Discipline: Clinical Research
Job type: Contract
Salary: £Day/ Hourly Rate: On application
Contact name: Roxanna Keshavarz

Contact email:
Contact phone: 01293584300
Job ref: 21073
Published: about 1 month ago
Expiry date: 11 April 2021


  • 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.

Day/ Hourly Rate: On application