Clinical Research Coordinator

Job Title: Clinical Research CoordinatorLocation: New York, NY 10021Type: Contract (1 Year Assignment)Start Date: 06/22/2026End Date: 06/18/2027Schedule: Monday – Friday | 9:00 AM – 5:00 PM ESTHours: 37.5 Hours per WeekCompensationPay Rate: $43 – $46 per hourJob Summary:We are seeking a detail-oriented Clinical Research Coordinator to support clinical research studies by collecting, managing, and ensuring the accuracy of human subject data. This role involves working with clinical databases, electronic medical records, and research protocols to ensure high-quality data collection and regulatory compliance.Key Responsibilities:Data Collection & ManagementCollect and abstract data from medical records, lab results, publications, and external physician officesEnter and maintain accurate data in research systems (e.g., Medidata, REDCap, CTMS, sponsor CRFs)Ensure data completeness, accuracy, and compliance with study protocolsPerform data queries and resolve missing or inconsistent informationSupport recruitment, consent, and data collection for selected non-therapeutic studies (as needed)Clinical Research OperationsRegister patients and track study visits using Clinical Trial Management Systems (CTMS)Participate in protocol training, CRA training, and departmental research meetingsSupport monitoring visits and audits from sponsors and internal QA teamsReporting & AnalysisGenerate progress reports for Principal Investigators, sponsors, IRB, DSM committees, and study teamsAssist in consolidating and analyzing study data for presentations or reportingProvide real-time updates on data entry and study progressCommunicate issues related to missing or incomplete data to the study teamQuality & ComplianceEnsure compliance with HIPAA and research regulatory standardsRedact sensitive information as requiredParticipate in quality assurance activities to maintain data integritySupport continuous improvement of data collection processesRequired QualificationsHigh School Diploma or GEDMedical or research experience requiredBasic computer skills (databases, spreadsheets, word processing tools)Strong attention to detail and data accuracyAbility to abstract clinical information from recordsBeginner-level written communication and analytical skillsPreferred QualificationsBachelor’s Degree2–4 years of clinical or research experienceFamiliarity with clinical research systems (Medidata, REDCap, CTMS)Knowledge of medical terminologyCertified Clinical Research Coordinator (CCRC) certification (preferred)SkillsData Collection & Data EntryClinical Research & Medical TerminologyHIPAA ComplianceCTMS / REDCap / Medidata SystemsData Analysis & ReportingStrong Analytical & Communication SkillsMicrosoft Office (Excel, Word, etc.)Attention to Detail & Data AccuracyPride Health offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k) retirement savings, life & disability insurance, an employee assistance program, legal support, auto and home insurance, pet insurance, and employee discounts with preferred vendors.