Clinical Research Coordinator

3 weeks ago

Charlotte, United States Joint and Muscle Medical Care Full time

Benefits:

Competitive salary

Health insurance

Paid time off

About Us:

Joint and Muscle Research Institute is a private research company within the uptown Charlotte area. We are looking for an experienced Clinical Research Coordinator for a busy and growing clinical research site. The ideal candidate will have at least 2 years of experience as a clinical research coordinator.

Candidates must possess the following:

· Commitment to excellence and quality patient care · High organizational ability with strong attention to detail · Excellent time management · Critical thinker and problem solver · Ability to work without supervision · Ability to work with all personalities · Intermediate computer skills and prior electronic data capture use (preferred) · Certified Clinical Research Coordinator or Certified Clinical Research Professional (preferred)

Responsibilities include:

· Coordinate Clinical Studies adhering to the principles of ICH/Good Clinical Practice · Collect initial medical history from patients and other appropriate sources · Work as a cohesive team member coordinating assigned studies and backing up other studies as needed · Educate and provide information to patients, families, and community groups regarding clinical drug trials · Assist and support Recruitment Team with pre-screening activities including but not limited to review of daily physician schedules for potential patients, database scouring and contacting outside research referrals. · Attend Investigator Meetings and Site initiation visits as needed · Complete all study procedures per protocol including vital signs, phlebotomy, spirometry (preferred) review of AE’s/SAE’s, concomitant medication updates, dispensation of IP, preparation/dosing of IP, drug accountability, lab processing, and data entry. · Inventory, handle, and maintain accountability for all study supplies and investigational products

Responsible for regulatory submissions for assigned studies as well as maintenance of regulatory documents/ISF.

· Facilitate study monitoring visits and prompt resolution of all study related queries· Maintain professional and appropriate interactions with sponsors and all other study related personnel, patients, patient family members, and other JMMCRI staff· Other duties as assigned

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