Freelance Study Start-Up and Regulatory Specialist

​Responsibilities:

• 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

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Requirements:

• 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

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

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Day/ Hourly Rate: On application