Site Director - New York, United States - Mantell Associates

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 activitiesBuild out a large team of top manufacturing professionalsWork directly with the COO and board in overseeing successful delivery of projectsContinually lead the expansion of the facility and the wider businessSite Head

• Requirements:B.

A. or B.S.

required, advanced degree preferredMinimum of 3 years' experience in managing clinical trialsUnderstand regulatory requirements, as well as Good Clinical Practices (GCP), HIPAA and International Conference on Harmonization (ICH) guidelinesAble to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous mannerKnowledgeable in medical terminology to communicate with physician offices, pharmacists and laboratory staffAble to manage a staff of clinical professionals and create a productive, satisfying work environmentDemonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policyExcellent communication skills (interpersonal, written, verbal)Ability to perform overnight business travelGood organizational and interpersonal skillsAttention to detailExcellent 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 #J-18808-Ljbffr