PhD Associate CTM – Oncology & Radiopharm (Office-Based)

Medpace; Cincinnati (OH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Flexible work environment

Competitive PTO packages

Competitive compensation and benefits

Employee wellness initiatives

Discounted tuition for UC online programs

Job summary

A leading CRO in Cincinnati is seeking an Associate Clinical Trial Manager (aCTM) to join its Clinical Trial Management team. The role requires a PhD in Life Sciences and offers an opportunity for recent graduates to enter the industry with comprehensive training. Responsibilities include collaborating on global study activities, maintaining project reports, and managing study supplies. The position provides a supportive environment for growth and career advancement in clinical trial management.

Qualifications

• PhD in Life Sciences is required.
• Fluent in English with strong presentation and communication skills.
• Ability to thrive in a fast-paced and dynamic international team.

Responsibilities

• Communicate and collaborate on global study activities with team members.
• Ensure timely delivery of tasks accurately.
• Compile and maintain project-specific status reports.

Skills

Fluency in English

Communication skills

Organizational skills

Computer skills (Word, Excel)

Education

PhD in Life Sciences

Tools

Microsoft Excel

Job description

A leading CRO in Cincinnati is seeking an Associate Clinical Trial Manager (aCTM) to join its Clinical Trial Management team. The role requires a PhD in Life Sciences and offers an opportunity for recent graduates to enter the industry with comprehensive training. Responsibilities include collaborating on global study activities, maintaining project reports, and managing study supplies. The position provides a supportive environment for growth and career advancement in clinical trial management.