Site Director - CRO
Mantell Associates
OH, United States
Full-time
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.
Less than 1 hour ago