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.
Responsibilities:
* Coordinating project timelines for all Data Management activities
* Coordination of data transfers with the clinical database programmers, Project Manager and
external recipients;
* Coordinate system development and ongoing maintenance in collaboration with the MCL
programmers and MCL operational team;
* Validation review and documentation of database set-up and data transfers;
* Edit Check output review including review by Subject Matter Experts; and
* Coordinate overall Data Management by serving as contact for MCL team members and
external data management groups.
Qualifications:
* Bachelor's degree (required) in a health related field with strong attention to detail and working knowledge of Excel and Word
* 4-6 years of DM experience in a pharmaceutical or CRO setting preferred
TRAVEL: None
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