Lead Clinical Research Coordinator

Tribe Clinical Research; Spartanburg (SC); On-site; USD 34,000 - 55,000; Full time

Job summary

Tribe Clinical Research in Spartanburg, SC is seeking a Clinical Research Coordinator to lead and support Phase II–IV trials on site. The role requires strong clinical skills, accurate data handling, and effective communication with investigators, staff, and sponsors.

A candidate will perform medical record reviews, participant interactions, and document regulatory processes while ensuring adherence to ethical standards and study protocols.

Qualifications

• CMA Certification or willingness to complete.
• Blood Draw experience preferred.
• Medical and Clinical Research Terminologies.
• Exceptional attention to detail and accuracy.
• Data Management and Informatics.
• Adhere to Principles of Ethical Research Standards.
• Highly organized individual.
• Continuous learning mindset.

Responsibilities

• Medical Record Review
• Protocol compliance/documentation
• Patient relations
• Sponsor relations/communication
• Investigational Product/Drug Administration
• Maintenance of organized, complete study charts, and legible, accurate research documentation through written progress notes
• Submit all regulatory documents and correspondence to regulatory personnel in a timely manner.
• Identify protocol problems and inform TCR Research Team of problems limiting recruitment and work on strategies to overcome these problems.
• Maintain detailed drug accountability
• Coordinate and document in-service training for appropriate staff
• Oversee organization and workflow of trials with meticulous attention to detail and ordering of priorities
• Navigate sponsor and study issues to resolution
• Conduct ordering of all protocol required follow-up labs, tests, procedures, and medications accurately and per qualifications and delegation by PI
• Collaborate with attending Investigator and Principal Investigator to report serious adverse events to study sponsor and regulatory personnel within mandated timeframe
• Participate in weekly site meetings
• Communicate with other professionals via phone, email, and face-to-face meetings to ensure the whole clinical trial team stays informed.

Skills

CMA Certification

Blood Draw experience

Medical Terminology

Clinical Research

Job description

Tribe Clinical Research in Spartanburg, SC is seeking a Clinical Research Coordinator to lead and support Phase II–IV trials on site. The role requires strong clinical skills, accurate data handling, and effective communication with investigators, staff, and sponsors.

A candidate will perform medical record reviews, participant interactions, and document regulatory processes while ensuring adherence to ethical standards and study protocols.