Director of Proposal Writing

				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:

* Mentor/Lead Proposal Writers in the preparation of compelling, strategic proposals, rebids, and exhibits, including rigorous quality control and timeline adherence;
* Review RFPs, identify any capacity issues, and negotiate deadlines with Business Development Executives, as needed;
* Participate in pre-RFP client meetings;
* Partner with Business Development, Medical and Operational personnel to design effective proposals;
* Contribute strategic operational content to proposals;
* Review and revise proposal content as needed to ensure a clear, compelling strategy to execute the trial is articulated;
* Participate in client discussions and requests for information following delivery of proposal;
* Lead the enhancement of proposal development tools and processes;
* Stay abreast of latest industry tactics and strategies regarding proposal development; and
* May be responsible for other projects and responsibilities as assigned.

Qualifications:

* Bachelor's degree minimum, advanced degree preferred;
* Highly-proficient employee with strong leadership, writing and problem solving skills;
* 5+ years of project management/clinical trial management experience in clinical research;  CRO experience preferred;
* Must possess superior time management, planning and organizational skills, written and verbal communication skills, and quality decision-making skills;
* Advanced knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines; and
* Demonstrated ability to effectively interact face-to-face with Sponsors and represent company in outside settings.
			

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