Freelance Clinical Research Associate
R
RhoClinical Research
FranceContractMiddle
Salary not disclosed
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Job Details
- Languages
- English and local languages
- Experience
- At least 2 years
Requirements
- University degree in medicine, pharmacy, nursing or life science.
- At least 2 years of previous on-site monitoring experience in a CRO or Pharma company.
- Previous experience in preparation and submissions to Ethics Committees and Regulatory Authorities.
- Fluency in English and local languages.
- Strong written, verbal, and presentation skills.
- Valid driver license and ability to travel.
- Attention to detail and understanding of high-quality scientific standards.
- Previous freelancing experience is considered an advantage.
Responsibilities
- Manage all aspects of study site management including site selection, initiation, routine monitoring, close-out, and maintenance of study files.
- Ensure the quality and integrity of data and compliance with relevant SOPs and regulatory requirements.
- Conduct country and site feasibility.
- Prepare and submit documents to Ethics Committees and Regulatory Authorities.
- Assist in site contract management.
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