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

Medpace; München; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

An established industry player is seeking a motivated Associate Clinical Trial Manager to join their Clinical Trial Management team. This full-time, office-based role is ideal for recent PhD graduates eager to transition into the clinical research field. You'll receive comprehensive training while working closely with project coordinators and clinical trial managers on various clinical trial management activities. This position offers a unique opportunity to develop your career in the research and development of innovative therapeutics within a dynamic international environment. If you're ready to apply your academic skills in a practical setting, this is the perfect chance to make a meaningful impact.

Qualifikationen

• PhD required in Life Sciences with strong analytical and presentation skills.
• Ability to work in a dynamic international team environment.

Aufgaben

• Coordinate global study activities and ensure timely delivery of tasks.
• Compile project-specific status reports and manage study supplies.

Kenntnisse

Analytical Skills

Presentation Skills

Collaboration

Communication

Ausbildung

PhD in Life Sciences

Jobbeschreibung

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

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