Experienced Clinical Trial Project Manager

Medpace; Cincinnati (OH); On-site; USD 70,000 - 90,000; Full time

Job summary

Medpace, located in Cincinnati, Ohio, is looking for an experienced professional to manage clinical trials within their specialized facility. The role involves coordinating various project activities, overseeing staff, and ensuring compliance with Sponsor specifications while maintaining study integrity.

The ideal candidate will possess a Bachelor’s degree and over 5 years of experience in clinical trial management, with a deep understanding of medical terminology and clinical research practices.

Qualifications

• 5+ years of managing clinical trials.
• Broad knowledge of medical terminology and clinical research methodology.

Responsibilities

• Manage one or more projects according to Sponsor specifications.
• Coordinate project start-up, maintenance, and close-out activities.
• Track study status including patient status and safety issues.

Skills

Project management

Knowledge of medical terminology

Clinical research methodology

Education

Bachelor’s Degree

Job description

Job Summary

Medpace 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;
• 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.