Job description
Mantell Associates is partnered with a leading CRO in their search for a Site Director to join their team.
Site Director - Responsibilities:
Oversee day to day operations and GMP manufacturing activities
Build out a large team of top manufacturing professionals
Work directly with the COO and board in overseeing successful delivery of projects
Continually lead the expansion of the facility and the wider business
Site Head - Requirements:
B.A. or B.S. required, advanced degree preferred
Minimum of 3 years' experience in managing clinical trials
Understand regulatory requirements, as well as Good Clinical Practices (GCP), HIPAA and International Conference on Harmonization (ICH) guidelines
Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner
Knowledgeable in medical terminology to communicate with physician offices, pharmacists and laboratory staff
Able to manage a staff of clinical professionals and create a productive, satisfying work environment
Demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy
Excellent communication skills (interpersonal, written, verbal)
Ability to perform overnight business travel
Good organizational and interpersonal skills
Attention to detail
Excellent Computer Skills to include Word, Excel, PowerPoint, as well as proprietary applications unique to the clinical research industry (such as Study Manager)
Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at +1 (786) 485 1298.