Clinical Research Coordinator: Lead Study Coordination & Data

Reliance Clinical Testing Services, Inc.; Purchase (NY); On-site; USD 60,000 - 80,000; Full time

Job summary

ALS seeks aClinical Research Coordinator to plan, coordinate, and execute clinical studies, ensuring adherence to protocols and regulatory guidelines. You will manage study materials, consent processes, and data entry while supporting investigators and study teams.

Responsibilities include coordinating daily study activities, tracking participant attendance, and maintaining inspection-ready study records. The role requires collaboration across departments and a commitment to data integrity and

Qualifications

• Experience coordinating clinical research studies and ensuring protocol compliance.
• Understanding of Good Clinical Practice guidelines and regulatory requirements.
• Ability to collect, manage, and quality-check study data.

Responsibilities

• Plan, coordinate, and execute clinical research studies according to protocols and sponsor requirements.
• Prepare documents including consent forms, screening materials, and source documents.
• Monitor subject safety, document adverse events, and ensure accurate data entry.

Skills

Study coordination

Data management

GCP compliance

Education

Bachelor's degree in life sciences

Tools

EDC systems

Job description

ALS seeks aClinical Research Coordinator to plan, coordinate, and execute clinical studies, ensuring adherence to protocols and regulatory guidelines. You will manage study materials, consent processes, and data entry while supporting investigators and study teams.

Responsibilities include coordinating daily study activities, tracking participant attendance, and maintaining inspection-ready study records. The role requires collaboration across departments and a commitment to data integrity and