Job SummaryMedpace Clinical Pharmacology, a 96-bed facility specializing in early phase clinical trials, is led by a team of highly trained clinical researchers who are experts in the design, implementation, and analysis of Phase I - IIa studies. The Phase I Unit, functionally integrated with Medpace, a large global Clinical Research Organization, conducts studies and collaborates with the best therapeutic minds in the industry to bring promising drug compounds to the market.
Responsibilities- Responsible for managing one or more projects according to Sponsor specifications;
- Coordinate project start-up, maintenance, and close-out activities;
- Track study status including patient status, case report form status, safety issues, timelines, etc.;
- Serve as primary contact for all protocol interpretations and logistical project-related issues; and
- Provide oversight for staff conducting study-related responsibilities/procedures.
Qualifications- Bachelor's Degree and 5+ years of nanaging clinical trials; and
- Broad knowledge of medical terminology and clinical research methodology.
Cincinnati Perks- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
