Mantell Associates is partnered with a leading CRO in their search for a Site Director to join their team. ​

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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

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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)

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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.