Freelance CRA - Greece

Proclinical are seeking a Freelance Clinical Research Associate (CRA) in Greece with a strong background in start-up operations to join our boutique CRO's dynamic team. In this role, you will play a crucial part in the initiation and execution of clinical trials, ensuring compliance with regulatory standards and efficient site management.

This is a long-term project requiring 15-20 hours per week work.

Key Responsibilities:

1. Site Selection and Qualification: Identify and evaluate clinical trial sites, ensuring they meet all necessary requirements for study conduct.

2. Start-Up Procedures: Lead the start-up activities, including regulatory submissions, ethics committee approvals, and site initiation visits.

3. Monitoring and Quality Assurance: Conduct site visits to monitor study activities, verify data accuracy, and ensure adherence to the protocol and regulatory guidelines.

4. Documentation: Maintain and update study documentation, including essential documents and trial master files.

5. Risk Management: Identify and address potential risks and issues during the start-up phase, proactively finding solutions to ensure smooth trial initiation.

Qualifications:

• Proven experience as a Clinical Research Associate (CRA), preferably in a freelance capacity.
• Strong knowledge of clinical trial start-up processes and regulatory requirements.
• Excellent communication and organisational skills.
• Ability to work independently and collaborate effectively with cross-functional teams.
• Attention to detail and a commitment to maintaining data integrity.

If you are having difficulty in applying or if you have any questions, please contact Roy Nelson at +41 61 563 12 41.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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