Avacare is looking to solve the problem of leading clinical trial operations at their Kansas City site, driving clinical trial success through strategic oversight, operational excellence, and team development.
Requirements
- Hands-on clinical experience including obtaining vitals, performing blood draws, EKGs, etc.
- Extensive knowledge of GCP/ICH guidelines and clinical trial regulations
- Strong understanding of site operations and the drug development lifecycle
- Experience in leadership, project management, and process improvement
- Skilled in onboarding and training new team members, including Research Assistants and CRCs
- Proven success as a lead Clinical Research Coordinator (CRC) with experience managing concurrent studies
- Demonstrated ability to fulfill responsibilities equivalent to a CRC II or higher
Responsibilities
- Lead and manage site operations, including staff training and development
- Oversee multiple concurrent studies across various therapeutic areas
- Conduct regular 1:1 meetings and annual performance reviews
- Perform quality control checks and collaborate with Quality Assurance
- Manage scheduling and coordination of patient/research participant activities
- Ensure accurate source documentation, data entry, and query resolution
- Maintain compliance with study protocols, GCP/ICH, and regulatory requirements
Other
- Associate Degree or higher preferred
- Ability to work on site in Kansas City, MO
- Ability to collaborate cross-functionally
- Ability to participate in leadership and management training programs
- Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits
