Contract Manager

UK-London

International Careers

Req #: 12733
Type: Full-Time
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Medpace, Inc.

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				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 6,000 people across 40+ countries.

Responsibilities:

* End-to-end management of the clinical study agreement (CSA) process for global, multi-site clinical trials
* Develop the study-specific CSA strategy with the Sponsor and internal stakeholders
* Develop country-specific CSA templates
* Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines.

Qualifications:

* Bachelor's degree in life-sciences or relevant legal or business field;
* Clinical Trial experience;
* CRO experience preferred;
* International Contract and budget negotiation experience;
* 3+ years of management or oversight experience;
* Ability to effectively influence others;
* Exceptionally strong communication skills;
* Advanced knowledge of Microsoft Word, Excel, and PowerPoint.
			
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