Job Description

Job Title: Senior Clinical Research Coordinator

Location: 100 McGregor Street, Manchester, NH 03102

Schedule: Monday–Friday, 8:00 AM–5:00 PM (early start times may be required based on study needs)

Travel: None required

Position Summary

The Senior Clinical Research Coordinator (Sr. CRC) is responsible for managing multiple clinical research protocols while serving as a key liaison between investigators, site staff, and study sponsors. This role ensures compliance with regulatory requirements, patient safety, and efficient protocol execution, while also providing mentorship and guidance to junior coordinators.

Key Responsibilities

• Coordinate all operational aspects of clinical research studies from feasibility through study closeout
• Collaborate with investigators, site departments, IRB, and sponsors to ensure regulatory and protocol compliance
• Accurately document patient encounters, study data, and protocol-specific requirements in a timely manner
• Support patient enrollment, informed consent, follow-up scheduling, and data submission
• Assist with site development, performance monitoring, and process improvement initiatives
• Provide training, mentorship, and ongoing support to CRC I and CRC II staff

Qualifications

• Bachelor’s degree required; Master’s degree preferred
• Minimum of 1 year of clinical research experience required; 5+ years preferred
• ACRP or CCRP certification preferred
• Strong knowledge of ICH/GCP guidelines and federal regulations
• Excellent communication and organizational skills
• Proficiency in ECGs, phlebotomy, and specimen handling

Health & Compliance Requirements

• TB test within the past 3 months
• Proof of immunization or declination for the following:
• Tdap
• MMR
• Varicella
• Hepatitis B
• Seasonal influenza
• Respirator fit test

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