Clinical Research Coordinator

About the Company

The client is a mission-driven organization focused on advancing clinical research through high-quality trial execution and patient-centered care. The team partners closely with Investigators Sponsors and CROs to deliver compliant efficient studies while maintaining the highest standards of research integrity.

The environment is fast-paced collaborative and rooted in regulatory excellence and continuous improvement.

About the Role

The client is seeking a Clinical Research Coordinator (CRC) to support the day-to-day coordination and execution of clinical trials. This role is responsible for managing both participant-facing activities and clinical trial data ensuring all study operations align with protocols Good Clinical Practice (GCP) FDA regulations and company SOPs.

In this role you will work closely with Principal Investigators Sponsors CROs and clinical teams to ensure smooth study execution accurate data collection and a high-quality patient experience. This is an ideal opportunity for a CRC who thrives in a fast-paced regulated environment and enjoys balancing clinical responsibilities with data and operational oversight.

Key responsibilities include:

• Coordinate clinical trials under the supervision of the Principal Investigator
• Ensure compliance with study protocols GCP FDA regulations and SOPs
• Support participant screening eligibility review and informed consent processes
• Educate participants and families on study procedures and expectations
• Perform clinical procedures such as vital signs ECGs phlebotomy and specimen processing
• Maintain accurate source documentation regulatory files and study records
• Enter and manage data in EDC systems resolve queries and update CTMS
• Support recruitment efforts enrollment tracking and study startup activities
• Communicate effectively with Sponsors CROs monitors and internal teams
• Conduct quality control checks and support audit and compliance activities

This role may require flexibility to support multiple clinical sites and adapt to evolving study needs.

Requirements

Experience & Education

• Minimum 2 years of experience as a Clinical Research Coordinator or in a related clinical research role
• At least 1 year of experience in Psychiatry Neurology or CNS studies
• Experience working in GCP and FDA-regulated environments
• CCRC or CCRP certification preferred

Clinical & Technical Skills

• Experience performing clinical procedures (vital signs ECG phlebotomy specimen handling)
• Strong understanding of clinical trial processes protocols and regulatory requirements
• Experience with EDC systems CTMS and clinical documentation practices
• Knowledge of medical terminology and clinical practices

Core Competencies

• Strong organizational and multitasking skills in a fast-paced environment
• Excellent communication and interpersonal skills
• High attention to detail with strong critical thinking ability
• Ability to work collaboratively across clinical and operational teams
• Patient-focused mindset with professionalism and empathy
• Self-motivated with the ability to manage competing priorities

Additional Requirements

• Ability to work across multiple sites as needed
• Flexibility to adapt to changing study demands and timelines
• Commitment to quality compliance and research integrity