Freelance Clinical Research Associate
Rho
contract
Posted on:
Location: 🇫🇮 Finland
Visit company websiteJob Level
JuniorMid-Level
Tech Stack
Google Cloud Platform
About the role
- Manage all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files
- Ensure quality and integrity of data, compliance with SOPs and regulatory requirements, and study completion on time and within budget
- Site administration and site monitoring responsibility according to Dokumeds and Sponsor SOPs, legal requirements and ICH-GCP Guidelines
- Conduct country and site feasibility assessments
- Perform site initiation, routine monitoring and close-out visits
- Prepare and submit documents to Ethics Committees and Regulatory Authorities
- Assist in site contract management
Requirements
- University degree in medicine, pharmacy, nursing or life science
- At least 2 years of previous on-site monitoring experience in CRO or Pharma company
- Previous freelancing experience will be considered as an advantage
- Previous experience in preparation and submissions to Ethics Committees / Regulatory Authorities
- Strong Communicator: written, verbal and presentation skills; Fluency in both English and local languages
- Committed to Quality: attention to detail and high-quality scientific standards
- High-Character: honesty, integrity, team spirit, loyalty, accountability and mutual trust
- Critical Thinker: evaluate situations objectively and craft practical solutions
- Agile and Adaptable: ability to change quickly and manage risk
- Driver license and ability to travel
- CV must be submitted in English