Medix
Clinical Research Coordinator (CRC)
Charleston, South Carolina 29405 | Full-Time M-F 40 hours a week
Are you passionate about advancing medical research and improving patient outcomes? Join our dynamic team as a
Clinical Research Coordinator (CRC)
and be part of groundbreaking clinical studies that make a real difference. In this role, you’ll ensure clinical trials are conducted safely, ethically, and in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs.
Key Responsibilities Working closely with Site Managers, Principal/Sub Investigators, and the broader clinical research team, your responsibilities will include: Screening, consenting, and following up with study participants Documenting in source charts and entering data into EDC systems Obtaining vital signs, ECGs, and performing basic lab procedures (phlebotomy, specimen handling, etc.) Scheduling study visits, appointment reminders, and maintaining study logs Coordinating monitoring visits and ensuring timely resolution of findings Submitting SAE/deviation reports and ensuring investigator reviews are completed promptly Supporting study start-up activities and attending SIVs and Investigator Meetings Practicing ALCOAC documentation principles at all times Maintaining effective communication with patients, sponsors, and team members
Requirements Education & Experience: Medical Assistant diploma, LPN/LVN, EMT certification
OR
Associate's degree Minimum
1 year
of clinical research or clinical experience Equivalent education/experience combinations may be considered Preferred Skills: Clinical procedures: blood pressure, vitals, ECGs, phlebotomy Bilingual in English/Spanish is a
plus BLS certification preferred Technical Skills: Proficient in Microsoft Office, EHRs, and web applications Typing speed of at least 40 WPM Soft Skills: Exceptional attention to detail and organizational skills Excellent written/verbal communication Able to work independently and as part of a team Strong integrity, confidentiality, and work ethic Adaptability in fast-paced environments
Benefits We value our employees and offer a comprehensive benefits package for full-time team members (30+ hours/week), effective the first of the month after hire: Medical, dental, and vision insurance Life, short-term and long-term disability insurance Health Savings Account (HSA) Supplemental insurance options 401(k) with safe harbor match
Are you passionate about advancing medical research and improving patient outcomes? Join our dynamic team as a
Clinical Research Coordinator (CRC)
and be part of groundbreaking clinical studies that make a real difference. In this role, you’ll ensure clinical trials are conducted safely, ethically, and in compliance with GCP, ICH, HIPAA, FDA regulations, and SOPs.
Key Responsibilities Working closely with Site Managers, Principal/Sub Investigators, and the broader clinical research team, your responsibilities will include: Screening, consenting, and following up with study participants Documenting in source charts and entering data into EDC systems Obtaining vital signs, ECGs, and performing basic lab procedures (phlebotomy, specimen handling, etc.) Scheduling study visits, appointment reminders, and maintaining study logs Coordinating monitoring visits and ensuring timely resolution of findings Submitting SAE/deviation reports and ensuring investigator reviews are completed promptly Supporting study start-up activities and attending SIVs and Investigator Meetings Practicing ALCOAC documentation principles at all times Maintaining effective communication with patients, sponsors, and team members
Requirements Education & Experience: Medical Assistant diploma, LPN/LVN, EMT certification
OR
Associate's degree Minimum
1 year
of clinical research or clinical experience Equivalent education/experience combinations may be considered Preferred Skills: Clinical procedures: blood pressure, vitals, ECGs, phlebotomy Bilingual in English/Spanish is a
plus BLS certification preferred Technical Skills: Proficient in Microsoft Office, EHRs, and web applications Typing speed of at least 40 WPM Soft Skills: Exceptional attention to detail and organizational skills Excellent written/verbal communication Able to work independently and as part of a team Strong integrity, confidentiality, and work ethic Adaptability in fast-paced environments
Benefits We value our employees and offer a comprehensive benefits package for full-time team members (30+ hours/week), effective the first of the month after hire: Medical, dental, and vision insurance Life, short-term and long-term disability insurance Health Savings Account (HSA) Supplemental insurance options 401(k) with safe harbor match