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.