CRA Job at Precision Medicine Group | Apply Now
CRA job seekers looking for a remote opportunity in Europe can explore this exciting role at Precision Medicine Group. This life science job offers a unique chance to work in clinical research with a strong focus on oncology and rare diseases, while maintaining an excellent work-life balance.
- Job Position: Clinical Research Associate I / Clinical Research Associate II
- Location: France – Remote
About the Company
CRA job opportunities at Precision Medicine Group offer a unique experience compared to traditional CROs. Precision Medicine Group has integrated advanced technologies, scientific expertise, and operational scale to improve the speed, cost, and success rate of bringing life-changing therapies to patients. This life science job environment emphasizes oncology and rare diseases, combining clinical trial execution with laboratory expertise and advanced data sciences.
The company is known for its strong culture, high CRA retention rates, and a supportive work environment where employees enjoy a better quality of life and meaningful career growth.
Job Description
CRA job role involves monitoring and managing the progress of clinical studies at investigative sites. You will ensure that clinical studies are conducted, recorded, and reported in compliance with protocol, SOPs, ICH-GCP, and applicable regulations.
You will coordinate essential activities such as identifying investigators, preparing regulatory submissions, conducting pre-study visits, and initiation visits. This remote job requires travel for monitoring visits and offers a balanced workload with fewer protocols, enabling you to become a subject matter expert.
Qualifications
Minimum Required
CRA job candidates must meet the following criteria:
- Life science degree and/or equivalent experience
- Minimum 1 year experience as a CRA in CRO or pharmaceutical/biotech industry
- Experience managing oncology studies
- Site management or relevant clinical research experience
- Willingness to travel domestically with overnight stays
Other Requirements
CRA job applicants should demonstrate:
- Excellent communication and organizational skills
- Strong attention to detail
- Client-focused approach
- Ability to handle conflict effectively
- Fluency in English and local language (if applicable)
- Availability for up to 50–60% travel
Preferred
CRA job candidates with study start-up experience are preferred.
Key Responsibilities
CRA job responsibilities include overseeing clinical study progress and ensuring regulatory compliance at all stages.
- Monitor clinical studies at investigative sites
- Ensure studies are conducted as per protocol, SOPs, and ICH-GCP guidelines
- Coordinate study setup activities including investigator identification
- Support regulatory submissions and documentation
- Conduct pre-study, initiation, and monitoring visits
- Identify study risks and propose mitigation strategies
- Maintain accurate reporting and documentation
- Collaborate with project teams and stakeholders
Why Join Precision Medicine Group?
CRA job roles at Precision Medicine Group provide a supportive and growth-oriented environment. Employees benefit from:
- Lower number of protocols for better expertise
- Reasonable travel requirements
- Improved work-life balance
- Strong team culture and leadership support
- Opportunity to influence and make an impact
- Career growth in a leading life science job organization
