Site Director - CRO

Posted 02 April 2024
Salary Negotiable
Job type Full Time
Discipline CRO & Clinical Operations
Contact NameRobin Mantell

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.