Onsite Clinical Research Coordinator I – Patient-Centric Trials

Care Access; Georgia; On-site; USD 51,000 - 85,000; Full time

Benefits offered by this job

Paid Time Off

Company Holidays

Medical, Dental, Vision Insurance

Health Savings Account (HSA)

Flexible Spending Account (FSA)

401(k) with Company Match

Short-Term & Long-Term Disability

Job summary

Care Access seeks a Clinical Research Coordinator to conduct screening, enrollment, and monitoring of study subjects in alignment with GCP and sponsor requirements. You will obtain informed consent, maintain data integrity, and support regulatory documentation onsite across multiple visits.

Responsibilities include coordinating visits, performing basic procedures, reviewing test results, and ensuring patient safety and protocol adherence.

Qualifications

• Bachelor’s degree preferred, or equivalent combination of education, training, and experience.
• Minimum 1 year of Clinical Research Coordinator experience required.
• Recent phlebotomy experience required.
• Excellent knowledge of GCP, FDA regulations, and clinical terminology.
• Strong communication and documentation skills.

Responsibilities

• Screen, enroll, and monitor clinical study subjects in compliance with protocol.
• Obtain informed consent per SOPs and ensure patient privacy and safety.
• Perform basic procedures such as venipuncture, vitals, and ECGs.
• Maintain accurate data entry and source documentation with real-time updates.
• Coordinate site visits, liaise with sponsor/CRO, and report SAEs/AE promptly.
• Support recruitment planning and distribution of recruitment materials.
• Ensure regulatory and SOP compliance across all trial activities.

Skills

GCP knowledge

FDA regulations

Clinical terminology

Documentation

Communication

Education

Bachelor’s degree preferred

Tools

MS Word

MS Excel

EDC systems

IVR systems

Clinical trials database

Job description

Care Access seeks a Clinical Research Coordinator to conduct screening, enrollment, and monitoring of study subjects in alignment with GCP and sponsor requirements. You will obtain informed consent, maintain data integrity, and support regulatory documentation onsite across multiple visits.

Responsibilities include coordinating visits, performing basic procedures, reviewing test results, and ensuring patient safety and protocol adherence.