Chief Executive Officier - CEO (H / F)

NAOO (BATHWAVES); Villeneuve-d'Ascq; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

An innovative company is seeking a full-time Associate Clinical Trial Manager to join their Clinical Trial Management team. This exciting role offers recent PhD graduates a fantastic opportunity to enter the clinical research industry, receive comprehensive training, and develop their careers in the research and development of cutting-edge therapeutics. You will work closely with project coordinators and clinical trial managers, ensuring timely delivery of tasks and maintaining project status reports. This role promises a dynamic environment where your analytical skills will be valued, and you will have the chance to grow professionally within a supportive international team.

Prestations

Hybrid work-from-home options

Competitive PTO packages

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Competitive compensation and benefits package

Structured career paths for growth

Qualifications

• PhD required, with strong analytical and presentation skills.
• Ability to work in a fast-paced, dynamic international team.

Responsabilités

• Collaborate on global study activities with project teams.
• Ensure timely delivery of tasks with high accuracy.
• Maintain project-specific status reports.

Connaissances

Analytical Skills

Presentation Skills

Team Collaboration

Adaptability

Formation

PhD in Life Sciences

Description du poste

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our 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 across 40+ countries.

Why Medpace?

• Hybrid work-from-home options (dependent upon position and level)
• Competitive PTO packages
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO / AA Employer M / F / Disability / Vets