<p>Overview</p> <p>Clinical Research Coordinator (CRC)</p> <p>Location: Plymouth, MA | Site Name: Headlands Research - Eastern Massachusetts | Full-Time</p> <p>Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.</p> <p>We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Plymouth, MA. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.</p> <p>Type: Regular Full-time EmployeeSchedule: Mondays through Fridays, 8:00am - 5:00pmLocation: Onsite in Plymouth, MA (no capabilities for remote or hybrid work)Reports to: Senior Director of Regional OperationsBenefits: Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.</p> <p>What We Offer</p> <ul> <li>Competitive pay + annual performance incentives </li><li>Medical, dental, and vision insurance </li><li>401(k) plan with company match </li><li>Paid time off (PTO) and company holidays </li><li>A mission-driven culture focused on advancing medicine and improving patient outcomes </li></ul> <p>Why Join Us?</p> <p>You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.</p> <p>Responsibilities</p> <ul> <li>Coordinate all aspects of assigned clinical trials from site initiation to study close-out </li><li>Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards </li><li>Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs </li><li>Manage subject recruitment, informed consent, and retention strategies </li><li>Ensure timely data entry and resolution of EDC queries </li><li>Report and follow up on all adverse events, serious adverse events, and deviations </li><li>Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders </li><li>Prepare for and participate in monitoring visits, audits, and inspections </li><li>Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems </li><li>Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained) </li><li>Attend investigator meetings and provide cross-functional support as needed </li><li>Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control </li></ul> <p>Qualifications</p> <p>Education & Experience Requirements</p> <ul> <li>Required: High school diploma or GED </li><li>Preferred: Bachelor's degree </li><li>Experience: </li><li>Minimum 1 year of experience as a Clinical Research Coordinator </li><li>Industry-sponsored trial experience strongly preferred (CNS study experience a plus) </li><li>Previous hands-on patient care experience with memory disorder patients a plus </li><li>Familiarity with electronic data capture (EDC), IVRS, and other trial platforms </li></ul> <p>Skills & Qualifications</p> <ul> <li>Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures </li><li>Proficiency in medical terminology and clinical documentation practices </li><li>Strong interpersonal, verbal, and written communication skills </li><li>Organized, detail-oriented, and capable of managing multiple priorities </li><li>Proficient in Microsoft Office and other clinical research systems </li></ul> <p>Apply now to become a part of a team that's changing the future of healthcare-one trial at a time.</p>