Clinical Research Coordinator

Clinical Research Coordinator

The Clinical Research Coordinator plays a key role in the successful execution of clinical trials. This position coordinates all aspects of assigned studies, including patient recruitment, study procedures, documentation, and communication with investigators and sponsor representatives. This role is ideal for individuals who are detail‑oriented, organized, and motivated to grow within the clinical research field.

The Clinical Research Coordinator is responsible for identifying and assessing patients, distributing study information, serving as a resource for physicians, sponsor representatives, and patients, conducting follow‑up care, and attending all meetings related to assigned clinical trials.

Supports the daily operations of clinical trials by coordinating studies in accordance with site SOPs, Good Clinical Practice (GCP), FDA regulations, and all applicable federal guidelines.

- Conduct clinical research studies according to sponsor requirements, FDA regulations, and ICH/GCP guidelines

- Execute study procedures in alignment with each pharmaceutical sponsor’s protocol

- Document all study procedures and maintain accurate, complete source documentation

- Recruit, screen, and maintain patients for assigned studies

- Perform protocol‑related procedures as required

- Screen potential participants via phone and in‑office assessments

- Maintain accurate study medication accountability and documentation

- Keep investigators informed of patient status and any changes in medical condition not yet reported to the physician

- This position has NO supervisory responsibilities.

- Experience as a Clinical Research Coordinator preferred

- BS, BA, or LPN preferred

- Ability to perform all essential duties satisfactorily

- Strong attention to detail and organizational skills

- Excellent communication and interpersonal abilities

- Ability to read and interpret safety rules, operating instructions, procedure manuals, and clinical research materials (e.g., source documents, CRFs)

- Ability to write routine correspondence and progress notes

- Typing and computer proficiency required

- Ability to apply common‑sense understanding to carry out written, oral, or diagram‑based instructions

- Ability to manage problems involving several variables and outcomes

Job Type: Full-time

Pay: $45,000.00 - $60,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

People with a criminal record are encouraged to apply

Work Location: In person