Clinical Research Coordinator

The Role

Clinical Research Atlanta is seeking a Clinical Research Coordinator (CRC) to join our team in Stockbridge, Georgia. We are considering candidates at the CRC I, CRC II, or CRC III level, depending on experience and qualifications. The ideal candidate has previous hands-on experience as a Clinical Research Coordinator, understands clinical trial operations, and is passionate about delivering high-quality research and exceptional participant care.

Working under the supervision of the Site Director and in collaboration with Principal Investigators and other research professionals, the CRC will coordinate clinical research activities, ensure compliance with study protocols, and help maintain the integrity and quality of clinical trial data.

Key Responsibilities

• Coordinate clinical research studies in accordance with study protocols, Good Clinical Practice (GCP), FDA regulations, and applicable standard operating procedures.
• Manage study activities, including participant screening, enrollment, scheduling, study visits, and follow-up.
• Facilitate and document the informed consent process in accordance with applicable regulations and study requirements.
• Coordinate and perform protocol-required study procedures within the scope of training and qualifications.
• Maintain accurate and timely source documentation, electronic data capture (EDC) entries, and data query resolution.
• Support investigational product accountability, study supply management, and equipment maintenance.
• Collect, process, package, and ship laboratory specimens as required by study protocols and applicable training.
• Prepare for and support sponsor monitoring visits, audits, inspections, and study closeout activities.
• Maintain clear and professional communication with study participants, investigators, sponsors, CROs, and internal research teams.
• Monitor participant safety and promptly report adverse events, protocol deviations, and other study-related concerns according to established procedures.
• Depending on experience, independently manage assigned studies, assist with training less experienced coordinators, and contribute to improvements in site operations.
• Perform other related duties as assigned.

Required Qualifications

• Previous hands-on experience working as a Clinical Research Coordinator is required.
• Working knowledge of clinical trial operations, study protocols, and Good Clinical Practice (GCP).
• Experience coordinating participant visits, maintaining research documentation, and supporting clinical study activities.
• Familiarity with electronic data capture (EDC) systems and clinical research documentation.
• Strong organizational skills with the ability to manage multiple priorities and maintain accurate records.
• Excellent verbal and written communication skills.
• Strong attention to detail and a commitment to participant safety, regulatory compliance, and research quality.
• Ability to work collaboratively with investigators, research staff, sponsors, and study participants.

Preferred Qualifications

• Experience coordinating pharmaceutical-sponsored or industry-initiated clinical trials.
• Associate's or bachelor's degree in a healthcare, life sciences, or related field.
• ACRP or SOCRA certification (CCRC or CCRP).
• Medical Assistant, Phlebotomy, or other relevant clinical certification.
• Experience performing venipuncture, processing laboratory specimens, or managing investigational products.
• Experience independently managing clinical research studies from startup through closeout.
• Experience mentoring or training other clinical research team members.