Clinical Research Coordinator

Clinical Research Coordinator

Location: On-Site, Full-Time

Salary: $70,000-$85,000

This organization is a specialized clinical research services provider that supports the design, execution, and management of clinical trials across multiple therapeutic areas. It partners with pharmaceutical, biotechnology, and medical device sponsors to conduct studies efficiently and in compliance with regulatory and ethical standards. Services often span early‑phase through late‑phase trials and may include feasibility assessments, site operations, patient recruitment, data collection, and regulatory coordination.

Responsibilities:

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
• Complete all relevant, required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner
• Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills
• Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up

Requirements:

• Bachelor's degree and 2 years relevant experience in the life science industry OR
• Associate's degree with 4 years relevant experience in the life science industry OR
• High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year
• Clinical Research Coordinator experience
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
• Proficient ability to work independently, plan and prioritize with minimal guidance
• Excellent attention to detail, organization, and communication with varied stakeholders
• Ability to work as a team player with the ability to adapt to changing schedules and assignments