Associate Clinical Trial Manager (PhD) - Neuroscience / Ophthalmology

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

Descrizione del lavoro

Join a forward-thinking company as an Associate Clinical Trial Manager, where you will leverage your PhD and analytical skills to manage clinical trials. This full-time position offers a fantastic opportunity for recent graduates to receive foundational training and develop a career in the research and development of cutting-edge therapeutics. You will work in an international environment, collaborating with project coordinators and clinical trial managers to ensure the successful execution of clinical trials. If you're eager to accelerate your career in Clinical Trial Management, this role is perfect for you.

Competenze

• PhD in Life Sciences is required for the role.
• Fluency in English with strong presentation skills is essential.

Mansioni

• Collaborate on global study activities and ensure timely task delivery.
• Compile project-specific status reports and manage study supplies.

Conoscenze

Analytical Skills

Presentation Skills

Collaboration

Communication

Formazione

PhD in Life Sciences

Descrizione del lavoro

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

What to Expect Next

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

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