CRA Job at ICON Strategic Solutions | Apply Now
Looking for a CRA job with a leading global clinical research organization? ICON Strategic Solutions is hiring a Clinical Research Associate I (CRA I) for a sponsor-dedicated hybrid role in Paris, France. This exciting opportunity allows life sciences professionals to work across Phase I–III clinical trials in neurology, dermatology, oncology, and rare diseases while building a rewarding career with one of the world’s leading CROs.
- Job Position: Clinical Research Associate I (CRA I)
- Department: Clinical Monitoring
- Location: Paris, France
- Job ID: JR154532
About ICON Strategic Solutions
CRA job opportunities at ICON Strategic Solutions offer professionals the chance to work with one of the world’s leading healthcare intelligence and clinical research organizations. ICON supports pharmaceutical, biotechnology, and medical device companies by delivering high-quality clinical development services worldwide. The organization promotes innovation, diversity, collaboration, and long-term career growth while maintaining the highest standards of patient safety and regulatory compliance.
Professionals looking for ICON careers can benefit from working in a sponsor-dedicated environment, gaining deep therapeutic expertise and contributing to the success of global clinical development programs.
CRA Job Description
CRA job responsibilities involve supporting clinical trial monitoring activities for a dedicated global pharmaceutical sponsor. The Clinical Research Associate I will work across Phase I, II, and III clinical trials in neurology, dermatology, oncology, and rare diseases while ensuring efficient study execution and regulatory compliance. As part of this life sciences job, the successful candidate will collaborate with sponsors, study sites, investigators, and internal teams to maintain high-quality clinical trial operations.
Qualifications
CRA job applicants should possess:
- University degree in Life Sciences, or a related field.
- 6–12 months of clinical trial monitoring experience within a CRO.
- Working knowledge of ICH-GCP guidelines.
- Ability to review and evaluate medical data.
- Fluent French and English communication skills (written and spoken).
- Strong interpersonal and communication skills.
- Ability to handle queries professionally and efficiently.
- Willingness to travel approximately eight times per month.
CRA Job – Key Responsibilities
CRA job responsibilities include:
- Coordinate the set-up and monitoring of clinical studies independently.
- Produce accurate study status reports.
- Maintain complete study documentation.
- Resolve sponsor-generated queries efficiently.
- Support study cost-efficiency initiatives.
- Assist in preparing and reviewing study documentation.
- Contribute to feasibility assessments for new study proposals.
- Build and maintain strong relationships with sponsors, investigators, and study site staff.
- Ensure patient safety through compliance with ICON procedures, study protocols, and regulatory requirements.
- Work collaboratively with internal teams and external stakeholders throughout the clinical trial process.
CRA job opportunities at ICON Strategic Solutions provide an excellent pathway for professionals seeking to advance their careers in clinical research. With exposure to global clinical trials, sponsor-dedicated projects, strong professional development, and comprehensive employee benefits, this Clinical Research Associate I position in Paris offers an ideal opportunity for candidates passionate about clinical development. If you are searching for ICON careers, a rewarding job in Paris, or your next life sciences job, this role is worth exploring.
