Phase I Clinical Trial Coordinator (Office-Based)

Medpace; Cincinnati (OH); On-site; USD 65,000 - 75,000; Full time

Job summary

Medpace is seeking an office-based Clinical Project Coordinator to join our Clinical Pharmacology Unit (CPU) to support the development of new medicines and therapies. In this role, you will work directly with Project Managers to support the day to day activities of Phase I clinical trials.

If you are looking for a fast paced, collaborative work environment, then this is the opportunity for you. Responsibilities include maintaining project-related files, IRB submissions, data entry,

Qualifications

• Excellent oral and written communication skills.
• Broad knowledge of medical terminology and clinical research methodology.

Responsibilities

• Provide day-to-day departmental/project support activities, such as maintenance of project-related files and IRB document preparation and submissions.
• Data entry into Medpace proprietary systems and Excel spreadsheets.
• Coordinate and provide minutes for department/project meetings or conference calls.
• Maintain spreadsheets and compile reports; and
• Perform other tasks as needed.

Skills

Oral and written communication

Medical terminology knowledge

Clinical research methodology

Education

Bachelor's degree in science or health-related field

Job description

Medpace is seeking an office-based Clinical Project Coordinator to join our Clinical Pharmacology Unit (CPU) to support the development of new medicines and therapies. In this role, you will work directly with Project Managers to support the day to day activities of Phase I clinical trials.

If you are looking for a fast paced, collaborative work environment, then this is the opportunity for you. Responsibilities include maintaining project-related files, IRB submissions, data entry,