Clinical Research Coordinator — Patient-Focused Trials

Socket.dev; Raleigh (NC); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Paid time off (PTO)

Health, dental, vision insurance

401(k) with company match

Employer-paid disability

Job summary

Care Access is seeking a Clinical Research Coordinator to screen, enroll, and monitor study subjects in accordance with GCP and regulatory requirements. You will coordinate regulatory documents, ensure protocol adherence, and support patient recruitment at onsite locations.

The role requires a Bachelor’s degree (preferred) or equivalent experience, with at least 1 year in a Clinical Research Coordinator role and recent phlebotomy experience.

Qualifications

• Bachelor’s degree or equivalent combination of education, training and experience.
• Minimum 1 year of Clinical Research Coordinator experience.
• Recent phlebotomy experience required.

Responsibilities

• Screen and enroll study subjects per protocol and regulatory requirements.
• Obtain informed consent per SOP and follow GCP.
• Coordinate regulatory documents and site visits.
• Record data in paper or electronic systems in real time.
• Review lab results, ECGs and other tests for completeness and timely investigator review.
• Recruit participants and assist in development of recruitment plans.
• Maintain SOP adherence and protocol timelines.
• Communicate clearly with investigators, sponsor representatives and site staff.

Skills

SOPs knowledge

GCP regulations

Clinical terminology

Data entry accuracy

Communication across diverse teams

Attention to detail

MS Word & Excel

Independent work

Education

Bachelor's degree preferred

Clinical Research Coordinator experience

Phlebotomy experience

Tools

Clinical trials database

IVR systems

EDC systems

Job description

Care Access is seeking a Clinical Research Coordinator to screen, enroll, and monitor study subjects in accordance with GCP and regulatory requirements. You will coordinate regulatory documents, ensure protocol adherence, and support patient recruitment at onsite locations.

The role requires a Bachelor’s degree (preferred) or equivalent experience, with at least 1 year in a Clinical Research Coordinator role and recent phlebotomy experience.