Project Coordinator, Data Monitoring - Entry Level

at  Medpace Inc

Job Summary :
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Entry Level Project Coordinator to join our Global Internal Data Monitoring team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
At Medpace, Project Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities :

• Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review of safety and efficacy data for ongoing trials
• Act as a liaison between Clinical Operations, Sponsors, and DMC and SAC members
• Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes)
• Assist in the development and maintenance of study specific documents describing DMC processes and procedures
• Maintain the study blind and handle unblinded materials with discretion to ensure confidentiality

Qualifications :

• Bachelor’s degree in life science or health related field
• General knowledge of medical terminology and drug development process
• Excellent written and verbal communication skills
• Proficient knowledge of Microsoft Word, Excel, and PowerPoint

TRAVEL: None
Training is available for entry-level candidates.
Medpace Overview :
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Why Medpace? :
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

• Partner with the Independent Data Monitoring Manager to identify and contract independent physicians and industry experts to assemble Data Monitoring Committees (DMCs) to review of safety and efficacy data for ongoing trials
• Act as a liaison between Clinical Operations, Sponsors, and DMC and SAC members
• Provide administrative, logistical, and coordinating support for DMCs (including scheduling meetings, distributing unblinded data, and documenting decisions and outcomes)
• Assist in the development and maintenance of study specific documents describing DMC processes and procedures
• Maintain the study blind and handle unblinded materials with discretion to ensure confidentialit