Clinical Scientist - R&D Pharma- F/M

Pierre Fabre Laboratories; Toulouse; Hybride; EUR 55 000 - 75 000; Plein temps

Avantages offerts par ce poste

Incentives

Profit-sharing

Health and provident insurance

16 days of RTT holidays

Public transport participation

Résumé du poste

Pierre Fabre Laboratories is seeking a Clinical Scientist – R&D Pharma to support clinical monitoring within oncology clinical trials. You'll provide insights during study meetings, analyze clinical data, and collaborate with various medical teams.

The ideal candidate will hold an advanced scientific degree and have at least 3 years of Pharma R&D experience, with proficiency in English. The position allows for up to 2 days of teleworking per week and includes an attractive benefits package.

Qualifications

• Experience in clinical trial development in oncology.
• Ability to synthesize literature and clinical insights.
• Familiarity with clinical study design and documentation.

Responsabilités

• Support Clinical Medical Monitoring activities.
• Provide insights in study level meetings and investigator interactions.
• Contribute to clinical documents such as protocols and study reports.

Connaissances

Proficiency in English (written and spoken)

3 years of experience with Pharma R&D

Formation

Advanced degree in a scientific discipline (e.g., PhD, PharmD, NP, PA)

Description du poste

We are looking for a Clinical Scientist – R&D Pharma to support Clinical Medical Monitoring activities in the framework of clinical trial development in oncology. The Clinical Development team focuses on oncology clinical development, strategic assessments and support to clinical trials.

In this position, you will support Pierre Fabre clinical team and development function through knowledge of investigator relationships and analysis of the clinical trials data.

Your role within a pioneering company in full expansion

At study level, and as directed, provide insights in internal study level meetings, investigator interactions, medical data review, curation and interpretation of aggregate PD, PK, efficacy, safety data, and as requested, contribute to author/review of study‑related documents and submissions.

Strategic Contributions

• Collaborate with the Clinical Development Director to synthesize literature, preclinical data, regulatory guidance, and clinical insights to build program rationale.
• Support the Clinical Development Director in proposals at advisory boards, investigator meetings, and site initiations.
• Stay current with the clinical landscape by attending scientific and clinical conferences.

Clinical Study Support

• Contribute to study design and develop clinical documents (e.g., protocols, investigator brochures, informed consent forms, study manuals, clinical study reports).
• Work closely with Medical Monitors and Clinical Operations to address protocol questions from health authorities and ethics committees.
• Participate in clinical site and vendor selection.
• Provide clinical status updates and build collaborative relationships with investigators and key opinion leaders (KOLs).

Operational Excellence

• Assist in organizing clinical meetings (e.g., advisory boards, data safety monitoring boards, and steering committees).
• Engage with Clinical Operations for site start-up, engagement, and recruitment.
• Support medical monitoring activities, and data quality reviews.

Cross‑Functional Collaboration

• Act as a task force leader for best practices or special initiatives.
• Represent the asset team at governance reviews and present on special topics.
• Work closely with external consultants, regulatory teams, and CROs to ensure program alignment.

This position is compatible with teleworking up to 2 days a week according to company rules.

We offer an attractive remuneration/benefits package: incentives, profit‑sharing, Pierre Fabre shareholding with matching contribution, health and provident insurance, 16 days of holidays (RTT) in addition to 25 days of personal holidays, public transport participation...

Your skills at the service of innovative projects

• Advanced degree in a scientific discipline (e.g., PhD, PharmD, NP, PA, or equivalent)
• 3 years of experience with Pharma R&D
• Proficiency in English (written and spoken)