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Associate Director Clinical Operations Biotech Jobs in Oklahoma

TalentCraft

Director Clinical Operations

Yukon, OK · On-site

The Regional Director of Clinical Operations is responsible for overseeing site performance, revenue generation, and quality of research conducted. The Regional Director of Clinical Operations is ...

New

Revitalize Nutrition Corp

Clinical Director

Oklahoma City, OK · On-site

$74K - $101K/yr

You will lead and develop the team, oversee clinical operations, strengthen client consultations ... The Clinic Director is accountable for the clinic's people, performance, culture, client experience ...

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Director Clinical Operations

TalentCraft

Yukon, OK • On-site

Other

Posted 2 days ago

New

Job description

The Regional Director of Clinical Operations is responsible for overseeing site performance, revenue generation, and quality of research conducted. The Regional Director of Clinical Operations is responsible for holding sites accountable to KPIs and revenue goals. The Regional Director is responsible assisting site in mitigating business risks and for reporting progress and risks to the Executive Director.


Reports to: Executive Director/COO


Job Description:


  • Strategically track and assess study start up performance and provide feedback to ensure successful start-up for revenue production and future business
  • Strategically assess site revenue production and provide feedback to meet revenue goals
  • Hold sites accountable to adequate scheduling to meet/exceed recruitment and revenue goals
  • Provide oversight of sites to ensure site is amply staffed and that staff are trained to meet study conduct requirements
  • Provide oversight of sites to ensure the site is equipped for study conduct
  • Provide oversight of sites are completing visits, edc, queries according to contractual terms
  • Support sites as a resource for clinical research questions
  • Ensure sites are conducting QC at site level and enlists the help of QA when needed for audits, inspections, or other QA needs
  • Interact with managers and PIs to make sure sites have ample investigator coverage
  • Communicate and verify site goals with manager and PI
  • Report site performance progress and risks to Executive Director and/or COO
  • Provide solutions for mitigating business risks
  • Other duties as assigned


Required Skills/Abilities:


  • Knowledge in the following areas:
  • Regulatory
  • Project Management
  • Clinical procedures
  • Sponsor interaction
  • Human Resources


Education and Experience:


  • College or Specialized Degree
  • 7-10 years’ experience in the Clinical Research Industry
  • 5+ years experience in supervisory/management role

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