Clinical Research Coordinator

EPM Scientific; Marlton (NJ); On-site; USD 70,000 - 85,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

3–4 weeks PTO

Job summary

EPM Scientific in Marlton, NJ is seeking a Clinical Research Coordinator to manage day-to-day activities for CNS trials across Phases 1–4, supporting recruitment, visits, and data collection.

The role emphasizes protocol adherence, GCP, and collaboration with sponsors and site staff to ensure accurate documentation and compliant trial execution.

Compensation includes $70,000–$85,000 base with a performance-based bonus, plus comprehensive benefits such as health, dental, vision, and 3–4 weeks PTO.

Qualifications

• 1–3+ years of experience as a Clinical Research Coordinator or similar role
• Prior experience at a clinical research site preferred
• Exposure to CNS/psychiatry trials preferred
• Ability to manage multiple protocols and priorities effectively
• Strong communication and patient-facing skills
• Phlebotomy or lab processing experience is a plus

Responsibilities

• Coordinate day-to-day activities for Phase 1-4 clinical trials within CNS and related therapeutic areas
• Support patient recruitment, screening, enrollment, and retention efforts
• Conduct study visits in accordance with protocol, GCP, and site SOPs
• Maintain accurate and timely source documentation, CRFs, and regulatory files
• Schedule and manage subject visits, including follow-up and data collection
• Collaborate with investigators, sponsors, CROs, and site staff to ensure smooth study execution
• Assist with site monitoring visits, audits, and query resolution
• Ensure compliance with ICH-GCP guidelines and applicable regulatory requirements
• Support lab sample processing, tracking, and shipment as needed

Skills

Strong communication

Patient-facing

Job description

Clinical Research Coordinator (CRC) - Marlton, NJ

Compensation

$70,000-85,000 base + performance-based bonus

• Comprehensive benefits package including health, dental, vision
• 3-4 weeks PTO + paid holidays

Company Overview

A fast-growing clinical research site network focused on advancing neuroscience and psychiatric therapeutics through high-quality clinical trial execution. With multiple active and upcoming studies across CNS indications, the organization partners closely with sponsors and CROs to bring innovative treatments to patients. Known for its patient-centric approach, experienced investigators, and strong site infrastructure, the company offers an excellent environment for clinical research professionals looking to deepen therapeutic and operational expertise.

Responsibilities

• Coordinate day-to-day activities for Phase 1-4 clinical trials within CNS and related therapeutic areas
• Support patient recruitment, screening, enrollment, and retention efforts
• Conduct study visits in accordance with protocol, GCP, and site SOPs
• Maintain accurate and timely source documentation, CRFs, and regulatory files
• Schedule and manage subject visits, including follow-up and data collection
• Collaborate with investigators, sponsors, CROs, and site staff to ensure smooth study execution
• Assist with site monitoring visits, audits, and query resolution
• Ensure compliance with ICH-GCP guidelines and applicable regulatory requirements
• Support lab sample processing, tracking, and shipment as needed

Qualifications

• 1-3+ years of experience as a Clinical Research Coordinator or similar role
• Prior experience at a clinical research site (preferred)
• Exposure to CNS/psychiatry trials (highly preferred)
• Ability to manage multiple protocols and priorities effectively
• Strong communication and patient-facing skills
• Phlebotomy or lab processing experience is a plus