Senior Clinical Scientist (Level 3+) M/F - Full Remote
Within our consulting firm, we support major players in healthcare, biotechnology, and the pharmaceutical industry in the development, monitoring, and market launch of major therapeutic innovations. As part of a strategic reinforcement of our client's clinical studies teams, we are looking for a Senior Clinical Scientist (Level 3 minimum). Mission in Full Remote (100% teleworking).
YOUR MISSIONS:
Integrated into the clinical development team, you would lead the scientific dimension of international clinical trials, from strategic framing to the valorization of results:
- Scientific Design and Development of Trials
- Preparation, writing, and revision of fundamental study documents (clinical protocols, investigator brochures, analysis plans, regulatory dossiers).
- Definition and validation of scientific, medical, and safety endpoints.
- Continuous analysis of scientific and medical literature to support the strategic choices of the development program.
- Scientific Monitoring and Data Surveillance
- In-depth analysis and continuous scientific review of clinical and safety data (safety data review, signal detection, medical consistency).
- Close collaboration with Data Management, Biostatistics, Pharmacovigilance, and medical research teams to guarantee the integrity of results.
- Participation in the writing of Clinical Study Reports (CSR) and recommendations for expert committees/independent reviews (DSMB).
- Coordination and Transversal Expertise
- Scientific point of contact for investigators, clinical operational teams, and regulatory authorities.
- Contribution to the preparation of regulatory submissions and scientific communications (publications, congresses).
Education and Experience:
Education: Higher scientific university degree (Doctorate / Ph.D., Pharm.D. or M.D.) in the field of life sciences, health, or pharmacology.
Experience: Senior Level / Level 3 minimum with solid and proven experience as a Clinical Scientist in the pharmaceutical industry, biotechnology, or in a CRO on Phase II to IV trials.
Skills and Languages:
Clinical Expertise: Perfect mastery of the conduct and scientific rigor of international clinical trials, GCP standards, and regulatory requirements (ICH).
Data Analysis: Demonstrated ability to interpret complex medical and biological data.
Fluent English (Mandatory): Perfect mastery of scientific English, both oral and written, indispensable for leading international meetings and writing study documentation.
Soft Skills:
- Complete autonomy and methodological rigor, indispensable for an activity conducted 100% remotely.
- Exceptional analytical and synthesis skills.
- Excellent communication and interpersonal skills to interact with global multidisciplinary project teams.
Do you wish to put your scientific rigor at the service of large-scale international clinical projects with full autonomy? Apply today!