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:
* Contribute directly to the growth and strategic development of a large, global Study Start-Up team;
* Develop and identify continuous improvement opportunities of internal processes;
* Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;
* Provide input on new business development opportunities; and
* Develop and maintain relationships with clients.
Qualifications:
* Bachelor's degree in Life Sciences or related field, Advanced degree is preferred;
* 8+ years as a study start-up senior leader within a CRO;
* Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;
* Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;
* Excellent written and oral communication; and
* Experience managing and developing a team.
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