Clinical Research CoordinatorAt Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.Clinical Research Coordinator (CRC)Location: Pikesville, MD | Site Name: Headlands Research - Pharmasite | Full-TimeAre 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.We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Pikesville, MD. 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.Type: Regular Full-time Employee Schedule: Mondays through Fridays, 8:00am - 5:00pm Location: Onsite in Pikesville, MD (no capabilities for remote or hybrid work) Reports to: Site Director Benefits: 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.What We OfferCompetitive pay + annual performance incentivesMedical, dental, and vision insurance401(k) plan with company matchPaid time off (PTO) and company holidaysA mission-driven culture focused on advancing medicine and improving patient outcomesWhy Join Us?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 fasterwhile 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.Responsibilities:Coordinate all aspects of assigned clinical trials from site initiation to study close-outConduct subject visits and ensure timely, accurate documentation following ALCOA-C standardsMaintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPsManage subject recruitment, informed consent, and retention strategiesEnsure timely data entry and resolution of EDC queriesReport and follow up on all adverse events, serious adverse events, and deviationsCollaborate with investigators, lab teams, sponsors/CROs, and internal stakeholdersPrepare for and participate in monitoring visits, audits, and inspectionsMaintain regulatory documentation and ensure proper training is completed for all study amendments and systemsExecute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)Attend investigator meetings and provide cross-functional support as neededMaintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory controlEducation & Experience RequirementsRequired: High school diploma or GEDExperience: Minimum of 1 year of experience as a Clinical Research Coordinator ORMinimum of 2 years of college within a health-related program ORLicensed as a Licensed Practical Nurse (LPN) or higher ORBachelor's degree in a health or scientific-related programSkills & QualificationsDeep understanding of FDA, ICH-GCP regulations, and clinical trial proceduresProficiency in medical terminology and clinical documentation practicesStrong interpersonal, verbal, and written communication skillsOrganized, detail-oriented, and capable of managing multiple prioritiesProficient in Microsoft Office and other clinical research systemsApply now to become a part of a team that's changing the future of healthcareone trial at a time.