Associate Clinical Trial Manager (PhD) - Radiopharmaceuticals

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

Résumé du poste

A leading clinical research organization in Lyon is seeking a full-time Associate Clinical Trial Manager. This role is ideal for recent PhD graduates in Life Sciences looking to enter the industry and develop their careers. Responsibilities include communicating with project teams, maintaining project statuses, and ensuring regulatory compliance. The position offers solid foundational training and an accelerated path in clinical trial management.

Qualifications

• PhD in Life Sciences required.
• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.

Responsabilités

• Communicate and collaborate on global study activities.
• Ensure timely delivery of recurrent tasks.
• Compile and maintain project-specific status reports.
• Interact with the internal project team and third-party vendors.
• Provide oversight and quality control of regulatory filing system.
• Create and maintain project timelines.
• Coordinate project meetings and produce quality minutes.

Connaissances

Fluency in English

Presentation skills

Ability to work in a fast-paced dynamic industry

Formation

PhD in Life Sciences

Description du poste

Medpace is currently seeking candidates with Radiopharmaceutical related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our France, Lyon Clinical 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 Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people