Oncology Clinical Trials Lead — Operations

Excelya; Saclay; Sur place; EUR 65 000 - 95 000; Plein temps

Avantages offerts par ce poste

Collaborative and inclusive environment

Opportunities to work on diverse projects

Exposure to leading experts in the field

Strong emphasis on personal growth and teamwork

Résumé du poste

A leading pharmaceutical CRO is seeking an Associate Project Manager to ensure the operational delivery of clinical studies, particularly in oncology trials. The role involves acting as the main interface among team members, managing study documents, overseeing financial aspects, and ensuring compliance with GCP regulations. Candidates should possess relevant operational experience in the pharmaceutical industry, a degree in a related field, and proficiency in French and English. This is a full-time position based in Saclay, Île-de-France.

Qualifications

• Operational experience in the pharmaceutical industry or a CRO (excluding internships).
• Proven experience in oncology clinical trials (Phases I preferred).
• Strong knowledge of GCP and clinical research regulations.
• Ability to manage multiple projects in parallel.
• Degree in Pharmacy, Engineering, Life Sciences (Bachelor's or Master's).
• Languages: French & English mandatory.

Responsabilités

• Ensure operational delivery of clinical studies from feasibility to site closure.
• Act as the main operational interface between CRAs and investigators.
• Contribute to the preparation and validation of study documents.
• Coordinate financial aspects of clinical studies.
• Oversee CRA activities and provide scientific support.
• Prepare and manage regulatory submission files.
• Ensure study quality and propose corrective actions.
• Organize investigator meetings and training sessions.
• Oversee pharmacovigilance activities.

Connaissances

Operational experience in the pharmaceutical industry

Experience in oncology clinical trials

Strong knowledge of GCP and clinical research regulations

Ability to manage multiple projects

Language proficiency in French and English

Formation

Degree in Pharmacy, Engineering, Life Sciences

Description du poste

A leading pharmaceutical CRO is seeking an Associate Project Manager to ensure the operational delivery of clinical studies, particularly in oncology trials. The role involves acting as the main interface among team members, managing study documents, overseeing financial aspects, and ensuring compliance with GCP regulations. Candidates should possess relevant operational experience in the pharmaceutical industry, a degree in a related field, and proficiency in French and English. This is a full-time position based in Saclay, Île-de-France.