Cra Ii/scra - Paris, France - Meet Recruitment
Description
45000 EUR EUR- Paris, France
- Permanent
Senior CRAs - Develop Your Career Towards CTL
- Are you passionate about advancing medical research and ensuring the highest standards of clinical trials?_
- Are you looking to progress your career towards a Clinical Trial Lead and explore your potential?_
As a Senior Clinical Research Associate, you will play a pivotal role in managing and supporting clinical trial sites, ensuring trials are conducted with utmost precision and adherence to protocols and quality standards.
Key Responsibilities:
- Maintain and ensure the accuracy of the Trial Master File (eTMF).
- Collaborate closely with Startup Specialists to facilitate EC and RA submissions.
- Independently conduct site evaluation, training, monitoring, and closure visits with a riskbased approach.
- Engage with project teams, startup teams, and management to ensure seamless communication.
- Generate accurate and timely reports, as well as handle issues and deviations effectively.
- Participate in work groups and take on additional tasks as needed.
Qualifications:
- Degree in medicine, pharmacy, or life sciences.
- Minimum of 3 years' experience as a CRA/SCRA with an emphasis on oncology.
- Profound knowledge of ICH-GCP guidelines.
- Fluent in French with advanced English skills (written and spoken).
- Proficiency in essential software tools (MS Excel, PowerPoint, Word, Outlook) and familiarity with study systems (eCRF, IVRS, ePRO, CTMS).
- Exceptional organizational skills with a keen attention to detail.
- Valid driver's license.
Why Us?
We are committed to integrity, innovation, transforming lives, community service, and embracing diversity and inclusion.
We value our employees and promote a collaborative and inclusive work environment where everyone's contributions are recognized and appreciated.
How to Apply:
If you are a dedicated Clinical Research Associate ready to make a difference, we invite you to join us in our mission.
