Associate Clinical Trial Manager (PhD) - Infectious Disease / Immunology

Medpace; Milano; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a dedicated Associate Clinical Trial Manager to join their Clinical Trial Management team. This is an exciting opportunity for recent PhD graduates to transition into the industry, where they will receive comprehensive training and work in a dynamic international environment. The role involves managing clinical trial activities, collaborating with various stakeholders, and ensuring the accuracy of project timelines and reports. If you have a passion for research and development in therapeutics and are ready to embark on an accelerated career path, this position is perfect for you.

Competenze

• PhD or Post-Doctoral Research experience required.
• Fluency in English and strong presentation skills needed.

Mansioni

• Manage global study activities and collaborate with project teams.
• Compile project-specific status reports and maintain timelines.

Conoscenze

Analytical Skills

Presentation Skills

Collaboration

Project Management

Formazione

PhD in Life Sciences

Strumenti

Clinical Trial Management System

Descrizione del lavoro

Job Summary

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
• Manage and perform 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