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About the Role

The Clinical Research Coordinator (CRC) supports the coordination and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional policies while protecting participant safety and data integrity. Working closely with Principal Investigators (PIs), research staff, and study participants, the CRC assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes.

Responsibilities

Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff
Conduct screening visits to collect medical history & other information from study participants
Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines
Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams
Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards
Communicate with study participants to provide education, answer questions, and support adherence to study requirements
Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team
Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines
Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified)
Scan, upload, file, and maintain organized study records and documentation
Apply critical thinking skills to support efficient study operations and problem resolution
Perform other duties as assigned

Requirements

High school diploma or equivalent required
Medical terminology & patient care experience required
Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities
Ability to communicate clearly and professionally with diverse populations
Ability to work collaboratively in a fast-paced, team-oriented environment
ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.

Skills

Basic knowledge of clinical research strongly preferred
Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred
Experience with participant screening and the informed consent process strongly preferred
Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred

Work Type

full-time
temporary

Education Level

associate’s degree or higher in a health-related field preferred

About the Company

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials.
We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care.
We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.