Clinical Research Coordinator

2 weeks ago

Charlotte, United States Joint and Muscle Medical Care Full time
Job DescriptionJob DescriptionBenefits:
  • 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 AEs/SAEs, 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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