Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)

Medpace; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a passionate Associate Clinical Trial Manager to join their dynamic team in Singapore. This full-time role is perfect for recent PhD graduates eager to dive into the world of clinical trial management, offering an exciting opportunity to work with cutting-edge radiopharmaceuticals. You'll receive comprehensive training and support while collaborating with a diverse international team. Your analytical skills will be put to the test as you manage project timelines, oversee study supplies, and ensure quality control in regulatory filings. If you're ready to accelerate your career in a fast-paced environment, this is the opportunity for you!

Qualifications

• PhD in Life Sciences with focus on nuclear medicine or related fields.
• Fluency in English with strong presentation and collaboration skills.

Responsibilities

• Collaborate on global study activities and ensure timely delivery of tasks.
• Compile project-specific status reports and maintain project timelines.

Skills

Analytical Skills

Presentation Skills

Collaboration

Project Management

Education

PhD in Life Sciences

Job description

Job Summary

Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. 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 radiopharmaceuticals. 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 (nuclear medicine/ radiopharmaceuticals/ radiation oncology or related)
• 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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