Clinical Trials Coordinator

Teak Research Consults specializes in Phase II- IV with two locations in Lawrenceville and Dunwoody GA

Job Summary
The Clinical Trials Coordinator is responsible for the day‑to‑day execution of clinical research activities in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. With a minimum of three years of hands‑on clinical trial coordination experience, this role ensures the smooth conduct of study visits, accurate documentation, timely data entry, and effective communication with participants, investigators, and study sponsors. The coordinator supports all operational aspects of assigned studies—including screening, enrollment, visit management, safety reporting, and regulatory compliance—while maintaining high standards of professionalism, organization, and participant care. This position requires strong attention to detail, the ability to manage multiple priorities, and a commitment to supporting high‑quality clinical research.

Responsibilities

• Coordinate all aspects of clinical trials, ensuring adherence to protocols and regulatory guidelines.
• Monitor patient progress and safety throughout the study, including conducting vital signs assessments and managing patient documentation.
• Review and maintain accurate documentation related to clinical trials, including data collection and management.
• Collaborate with cross-functional teams to ensure compliance with FDA regulations and standards.
• Handling, packaging, and shipping of processed lab samples
• Handling, storing, and processing study drug
• Creating source document
• Conduct patient recruitment, screening, and informed consent processes while adhering to HIPAA regulations.
• Manage clinical laboratory activities, including blood sampling and phlebotomy as required by the study protocols.
• Ensure proper training of staff on clinical trial procedures and compliance management.
• Informed consenting process
• Screening of research patient to determine eligibility
• Vast Knowledge in electronic Clinical Outcome Assessment

Qualifications

• 3+ years research experience
• Associates/ Bachelor's degree in a scientific, health related (preffered) or relevant experience in lieu of education
• Strong background in clinical trials management with knowledge of Good Clinical Practice (GCP).
• Familiarity with medical terminology, FDA regulations, and compliance requirements.
• Experience in documentation review, patient monitoring, data collection, and data management.
• Proficiency in using electronic medical record (EMR) systems and statistical software for data analysis.
• Skills in phlebotomy and blood sampling techniques.
• Excellent analytical skills with the ability to interpret complex data sets effectively.
• Knowledge of clinical development processes and the ability to work collaboratively within a research setting. This role is essential for advancing clinical research initiatives while ensuring the highest standards of patient care and regulatory compliance.
• Good communication, organization, and interpersonal skills
• Good computer skills including working knowledge of a PC and Microsoft office
• In depth knowledge of state and federal Regulatory guidelines related to research
• Applicants residing in the Atlanta area are strongly preferred.

Job Types: Part-time, Contract

Pay: From $24.00 per hour

Benefits:

• Referral program

Education:

• Bachelor's (Required)

Experience:

• Clinical research: 3 years (Required)
• Clinical trials management: 3 years (Preferred)

Ability to Commute:

• Lawrenceville, GA 30043 (Required)

Work Location: In person