A leading CRO for Biotech companies is seeking an Associate Clinical Trial Manager in Cincinnati, Ohio. This full-time position requires a PhD in Life Sciences and offers a supportive environment for developing your career in clinical project management. Responsibilities include communicating with a global team, ensuring timely project tasks, and overseeing regulatory filings. Medpace provides extensive training and competitive perks to help employees thrive in their roles.
Qualifications
Candidates should possess a PhD in Life Sciences.
Fluency in English with solid presentation skills is essential.
Excellent skills in word-processing, databases, and Excel are required.
Responsibilities
Coordinate with project coordinators and managers on study activities.
Compile and maintain project-specific status reports.
Manage project timelines and coordinate meetings.
Skills
Fluency in English
Organizational skills
Communication skills
Education
PhD in Life Sciences
Tools
Microsoft Word
Databases
Excel
Windows
Job description
A leading CRO for Biotech companies is seeking an Associate Clinical Trial Manager in Cincinnati, Ohio. This full-time position requires a PhD in Life Sciences and offers a supportive environment for developing your career in clinical project management. Responsibilities include communicating with a global team, ensuring timely project tasks, and overseeing regulatory filings. Medpace provides extensive training and competitive perks to help employees thrive in their roles.