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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Support clinical trial activities from study start-up to close-out, ensuring adherence to standards.
- Contribute to the preparation and review of trial protocols and amendments.
- Perform medical review of clinical data, including patient profiles and adverse event narratives.
- Collaborate with pharmacovigilance, clinical operations, and biostatistics teams for data review.
- Assist in medical writing and review of study-related documents.
- Ensure proper documentation and filing of study-related materials.
- Support preparation for audits, inspections, and regulatory submissions.
Requirements
What you’ll need- Experience in clinical research or related fields is beneficial but skills and motivation are prioritized.
- Strong analytical and clinical data review skills; collaboration in cross-functional teams.
- Familiarity with GCP and clinical trial regulations.
- Advanced degree in Life Sciences such as PharmD, MD, PhD, or MSc in Biology or related fields.
- Proficiency in English; knowledge of French is a plus.
Benefits
Comp & perks- We combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
- Unique employee experience and a young, ambitious health company.
- One-stop provider service model enabling diverse projects.
- Work alongside preeminent experts to enhance the patient's journey.
- Environment that values talents, pushes boundaries, and nurtures potential.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial activitiesmedical reviewdata reviewmedical writingdocumentationaudits preparationregulatory submissionsprotocol preparationadverse event narrativesclinical data analysis
Soft Skills
analytical skillscollaborationteamworkcommunication
Certifications
GCP
