Cardiovascular CTM (PhD) – Global Clinical Trials Associate
Medpace
Stirling
On-site
GBP 30,000 - 40,000
Full time
14 days+
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Job summary
Medpace is seeking a full-time Associate Clinical Trial Manager to join their Clinical Trial Management team in Stirling, Scotland. The role is ideal for recent PhD graduates in Life Sciences, offering foundational training and an entry into the pharmaceutical industry. Responsibilities include collaborating with global study teams, ensuring task accuracy, and maintaining project timelines. Candidates should possess strong analytical and communication skills, with fluency in English mandatory. This is a fantastic opportunity for career development in clinical trial management.
Qualifications
PhD in Life Sciences required.
Fluency in English with solid presentation skills.
Ability to work in a fast-paced dynamic industry.
Responsibilities
Communicate and collaborate on global study activities.
Ensure timely delivery of recurrent tasks.
Compile and maintain project-specific status reports.
Interact with internal project team and third-party vendors.
Provide oversight of internal regulatory filing system.
Create and maintain project timelines.
Coordinate project meetings and produce quality minutes.
Skills
Analytical skills
Collaboration
Communication
Presentation skills
Education
PhD in Life Sciences
Job description
Medpace is seeking a full-time Associate Clinical Trial Manager to join their Clinical Trial Management team in Stirling, Scotland. The role is ideal for recent PhD graduates in Life Sciences, offering foundational training and an entry into the pharmaceutical industry. Responsibilities include collaborating with global study teams, ensuring task accuracy, and maintaining project timelines. Candidates should possess strong analytical and communication skills, with fluency in English mandatory. This is a fantastic opportunity for career development in clinical trial management.