Clinical Research Coordinator Jobs

About The Position

Requirements

• 0–1 year of experience.
• Strong understanding of medical and clinical research terminology.
• Excellent verbal, written, and interpersonal communication skills.
• Exceptional attention to detail and accuracy.
• Proficiency in data management and informatics.
• Strong organization and time management skills, with the ability to multitask.
• Commitment to continuous learning and professional development.
• Ability to maintain confidentiality.
• Ability to understand and follow study protocols, including amendments, procedures, inclusion and exclusion criteria, and potential investigational product risks and side effects.
• Ability to travel among the Greer, Greenville, Simpsonville, and Spartanburg sites.
• Ability to lift up to 50 pounds and to sit, stand, and walk as required.
• Ability to work around potential exposure to fumes, airborne particles, infectious diseases, blood or bodily fluids, and disease-bearing specimens.

Nice To Haves

• Actively learning Good Clinical Practice (GCP), IATA standards, and standard operating procedures (SOPs).
• Begins CMA certification training if not previously completed.
• Checklist-based training in general clinical assessments and core research skills.
• Cross-training that includes phlebotomy and interdepartmental collaboration.

Responsibilities

• Recruit, screen, and assist with enrolling study participants according to protocol requirements.
• Obtain biological samples, process them, and arrange shipment as required by study and site needs.
• Collect, record, and maintain accurate study data in compliance with Good Clinical Practice.
• Conduct medical record reviews.
• Support participants throughout studies by answering inquiries, reinforcing study protocols, and escalating concerns to clinical staff when needed.
• Travel regularly among the Greer, Greenville, Simpsonville, and Spartanburg sites.
• Collaborate with investigators, clinicians, quality assurance personnel, and sponsors.
• Schedule and coordinate participant visits, assessments, and follow-ups.
• Input patient data into company systems.
• Organize trial workflow, prioritize work, and address sponsor and study issues through resolution.
• Maintain organized and complete study charts and legible, accurate research documentation, including written progress notes.
• Maintain working knowledge of study protocols, including their background, rationale, and investigational drug or device descriptions.
• Apply knowledge of inclusion and exclusion criteria and consult the Investigator with questions.
• Submit regulatory documents and correspondence to regulatory personnel in a timely manner.
• Identify protocol problems, inform the TCR Research Team of issues limiting recruitment, and work on strategies to address them.
• Participate in weekly site meetings.
• Facilitate clear communication among clinical trial teams through phone, email, and face-to-face interactions.
• Engage in cross-training, including phlebotomy and interdepartmental collaboration, to support patient procedures.
• Read and understand protocols and amendments, study procedures, and potential risks and side effects of investigational products.
• Interact with physicians, nurses, study monitors, sponsor representatives, administrators, employees, community resources, patients, and patients’ families and significant others.
• Adhere to ethical research principles, company core values, and applicable research standards and procedures.