Avacare is looking to solve the problem of conducting clinical research studies according to protocol, good clinical practice, and relevant local guidelines and regulations to support groundbreaking studies and improved patient outcomes.
Requirements
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Clinical Research Coordinator experience within a similar setting preferred
- Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
- Knowledge and experience of site operations and the drug development process
- Computer proficiency in use of Microsoft Word, Excel
Responsibilities
- Coordinate clinical research studies conducted by a supervising principle investigator.
- Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
- Obtains informed consent of research subjects
- Collects patient/research participant history
- Collects and maintains source documentation
- Manages inventory and administers test articles/investigational product to participants
- Performs data entry and query resolution
Other
- Develops strong working relationships and maintain effective communication with study team members
- Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines
- May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise
- Must be able to work on-site at the site in Kenner, LA
- Must be a team-oriented individual who thrives in a fast-paced setting
