Associate Clinical Trial Manager (PhD) - Oncology

Medpace, Inc.; Lyon; Sur place; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Flexible work environment

Competitive compensation and benefits

Structured career paths

Employee health and wellness initiatives

Résumé du poste

Medpace, Inc. is seeking an Associate Clinical Trial Manager for their Lyon, France office. This full-time role is ideal for recent PhD graduates with oncology-related research experience. The position includes a robust training program and offers growth opportunities within the clinical trial management team.

Responsibilities include overseeing study activities, maintaining project timelines, and ensuring compliance with quality standards. Candidates should possess a PhD in Life Sciences and effective communication skills for international collaboration.

Qualifications

• Desire to apply analytical and academic skills in clinical project administration.
• Experience working in a fast-paced, dynamic environment (not required but advantageous).

Responsabilités

• Collaborate on global study activities with project coordinator and clinical trial manager.
• Maintain project-specific status reports in the clinical trial management system.
• Coordinate project meetings and produce quality minutes.

Connaissances

Analytical skills

Presentation skills

Collaboration

English fluency

Formation

PhD in Life Sciences

Description du poste

Job Summary

Medpace is currently seeking candidates with Oncology related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, LyonClinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
• Compile and maintain project-specific status reports within the clinical trial management system
• Interact with the internal project team, Sponsor, study sites, and third-party vendors
• Provide oversight and quality control of our internal regulatory filing system
• Provide oversight and management of study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes

Qualifications

• PhD in Life Sciences
• Fluency in English with solid presentation skills
• Ability to work in a fast-paced dynamic industry within an international team
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives