Senior Clinical Research Associate
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Job Description
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Coordinating study setup, site monitoring, regulatory activities, clients, and junior CRA mentoring.
Responsibilities:
- Monitor and own the progress of clinical studies at investigative sites
- Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations and standards
- Coordinate activities required to set up and monitor studies, including identifying investigators, helping prepare regulatory submissions, and conducting pre-study and initiation visits
- Handle appropriately sized clinical trials
- Support larger clinical study teams
- Train and mentor junior staff members
- Interact directly with clients
- Initiate payments
- Participate in proposal activities, including development and client presentations
Requirements:
- 4-year college degree or equivalent experience
- Holder of CRA certificate
- Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
- Experience monitoring clinical trials across a variety of therapeutic areas
- Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment; international travel may be required for some senior level positions
- Fluency in English and the local language
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline preferred
- Study start-up activities experience preferred
- Understanding of financial management preferred for Senior CRAs
Benefits:
- Fully home-based within France
- Professional development
- Opportunity to build meaningful client relationships
- Career growth opportunities
- Empowerment to make an impact
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