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:
* Validate entry database designs
* Report metrics and data trends on projects
* Identify data conflicts and issues on projects
* Work with personnel from global research sites to resolve data conflicts
* Reconcile data from multiple sources
* Create and update study documentation on projects
* Participate as part of a team on various projects
Qualifications:
* PharmD or PhD required
* Bachelor's degree in a Life Science or related field with strong attention to detail, excellent communication skills, ability to prioritize and multitask effectively, and experience with Excel and Word.
* Previous experience working with research and statistical data is preferred ideally in a pharmaceutical or CRO setting.
Travel: None
Share this job:
Share this Job