Clinical Research Coordinator

Job Title: Clinical Research Coordinator Location: New York, NY 10021 Type: Contract (1 Year Assignment) Start Date: 06/22/2026 End Date: 06/18/2027 Schedule: Monday – Friday | 9:00 AM – 5:00 PM EST Hours: 37.5 Hours per Week Compensation Pay Rate: $43 – $46 per hour Job 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 & Management Collect and abstract data from medical records, lab results, publications, and external physician offices Enter and maintain accurate data in research systems (e.g., Medidata, REDCap, CTMS, sponsor CRFs) Ensure data completeness, accuracy, and compliance with study protocols Perform data queries and resolve missing or inconsistent information Support recruitment, consent, and data collection for selected non-therapeutic studies (as needed) Clinical Research Operations Register patients and track study visits using Clinical Trial Management Systems (CTMS) Participate in protocol training, CRA training, and departmental research meetings Support monitoring visits and audits from sponsors and internal QA teams Reporting & Analysis Generate progress reports for Principal Investigators, sponsors, IRB, DSM committees, and study teams Assist in consolidating and analyzing study data for presentations or reporting Provide real-time updates on data entry and study progress Communicate issues related to missing or incomplete data to the study team Quality & Compliance Ensure compliance with HIPAA and research regulatory standards Redact sensitive information as required Participate in quality assurance activities to maintain data integrity Support continuous improvement of data collection processes Required Qualifications High School Diploma or GED Medical or research experience required Basic computer skills (databases, spreadsheets, word processing tools) Strong attention to detail and data accuracy Ability to abstract clinical information from records Beginner-level written communication and analytical skills Preferred Qualifications Bachelor’s Degree 2–4 years of clinical or research experience Familiarity with clinical research systems (Medidata, REDCap, CTMS) Knowledge of medical terminology Certified Clinical Research Coordinator (CCRC) certification (preferred) Skills Data Collection & Data Entry Clinical Research & Medical Terminology HIPAA Compliance CTMS / REDCap / Medidata Systems Data Analysis & Reporting Strong Analytical & Communication Skills Microsoft Office (Excel, Word, etc.) Attention to Detail & Data Accuracy Pride 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.