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 approximately 3,500 people across almost 40 countries.
Our organization is rapidly growing and we are currently seeking full-time, office-based Regulatory Scientific Writers to join our Regulatory Affairs team. This position will work within a team structure to accomplish tasks and projects that are instrumental to the company's success. If you would like an exciting career where you use your scientific and clinical knowledge, then may be the opportunity for you.
Write clinical protocol synopses, clinical development plans, scientific advice documents, pediatric study plans, IND modules, NDA modules and other related regulatory documents;
Coordinate quality control reviews of those documents and maintaining audit trails of changes; and
Interact closely with the sponsor, and other Medpace subject matter experts.
Degree in a life science or engineering field (PhD, PharmD, or Advanced Degreed preferred, but not required);
3+ years of being primary author of INDs and NDAs
Strong computer skills, project management skills, and a high attention to detail; and
Strong communication skills (both written and oral).
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
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