Clinical Scientist- R&D Pharma - CDI- F/M

Pierre Fabre; Toulouse; Hybride; EUR 70 000 - 100 000; Plein temps

Avantages offerts par ce poste

Telework up to 2 days/week

Profit-sharing

Pierre Fabre shareholding

Health insurance

Provident insurance

16 RTT + 25 days personal holidays

Public transport participation

Résumé du poste

Pierre Fabre, a pioneering pharmaceutical company, seeks a Clinical Scientist- R&D Pharma to support oncology clinical development. You will contribute to investigator interactions, data review, and interpretation of PD, PK, efficacy, and safety data, while helping draft study documents and participate in advisory boards and site initiations.

The role emphasizes cross-functional collaboration, literature synthesis, and alignment with regulatory guidance.

Qualifications

• 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).

Responsabilités

• Support Clinical Medical Monitoring activities in oncology trials.
• Provide insights in study meetings, investigator interactions, and data interpretation.
• Develop clinical documents (protocols, brochures, ICFs, study manuals, CSRs).
• Collaborate with Medical Monitors and Clinical Operations on protocol questions.
• Assist in site and vendor selection and in governance reviews.

Connaissances

Investigator relationships

Clinical data analysis

Medical monitoring

Study design

Cross-functional collaboration

Formation

PhD or PharmD or equivalent

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 is based in Toulouse (Langlade) and 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...# Qui êtes-vous ?**Your skills at the service of innovative projects:**Advanced degree in a scientific discipline (e.g. PhD, PharmD, NP, PA, or equivalent) Oncology Field 3 years of experience with Pharma R&D Proficiency in English (written and spoken)