Clinical Research Coordinator Lead in Poughkeepsie, NY, United States Join our Talent Network Skip to main content Menu About us Benefits Culture Academics & Community Careers Nursing Careers Physicians & APP Careers Early Careers Medical Practice Careers Employees Job search Apply now Keyword, job title, skills Enter a Location Loading job Clinical Research Coordinator Lead Location: Poughkeepsie, NY, United States Salary Range: 33.21 - 61.68 Work Type: Full-Time Standard Hours: 40 FTE: Exempt Work Schedule: DAY 5 Work Shift: Monday - Friday, 8:30am - 5:00pm Date Posted: Apr 24, 2026 Share: Apply Now See what's possible in our system of care Nuvance Health extends from New York's Hudson Valley to western Connecticut. Our team of more than 15,000 caregivers delivers compassionate care through seven community hospitals, primary care and specialty practice locations, outpatient settings, home care services and telehealth visits. With strong hearts and open minds, we're pushing past boundaries and challenging the expected, all in the name of possibility. As we journey forward, we are guided by our values: personal, imaginative, agile and connected. Our curiosity is opening new pathways and creating new advancements in healthcare for all. Description Summary: Exhibits technical and functional expertise in the area of research/clinical trials through the execution of protocols for local and networkwide research. Coordinates daily activities of a designated study or group of studies and maintains industry relationships. Guides the training of physicians, fellows, and research staff on good clinical practice, external regulatory agency requirements. May be required to perform venipuncture on study participants; collects, processes, and ships specimens according to protocol and training requirements. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as necessary. Responsibilities: Responsible for coordination of a designated study or group of studies for single/multisite (networkwide). Evaluates trial protocols, manages the clinical research sites including, but not limited to acting as primary contact for clinical research sites for questions related to the protocol conduct protocol, regulatory document completion, study supplies, client scheduling, and electronic data capture. Trains, coaches, supports and mentoring, and day-to-day support of Clinical Research Coordinators and other team members. Keeps accurate and up-to-date records. Collects labels, logs, processes, and ships biological specimens for analysis according to protocol and training requirements. Schedules subjects for protocol-related evaluations; collaborates with physicians, investigators and other healthcare providers; promotes respect for subjects' rights. Provides on-site or remote monitoring of clinical research site activities to ensure compliance with protocols, SOPs and relevant federal and state regulatory and institutional policies. Provides consultation during study start-up activities regarding development of study protocol, SOP or Case Report Forms (CRFs), site qualification, data collection and study conduct. Participates in site initiations and trainings. Assesses accuracy, completeness and timeliness of study records by performing source data verification, regulatory document and consent form review, adverse event reporting compliance review, and investigational product accountability. Performs study close-out monitoring activities. Provides pre-review assistance prior to regulatory inspections and submissions. Promotes overall compliance and quality with research conduct through participation in education and training activities for professional staff. Assists in developing appropriate education and training sessions for investigators and clinicians involved in research. May provide technical guidance and direction to support team members, contractors and/or other vendors. 3-12 combined May travel to different clinical research sites as needed. Performs related duties, as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act. Duties not mentioned here, but considered related are not essential functions. Maintains and Models Nuvance Health Values. Demonstrates regular, reliable and predictable attendance. Requirements: Bachelor''s Degree required, or equivalent combination of Associate's degree and experience, required. 3-5 years of relevant experience, required. Venipuncture technique preferred, specimen handling and labeling Knowledge of blood collection procedures Salary Range: $33.21 - $61.68 Hourly, commensurate with experience With strong hearts and open minds, we're pushing past boundaries and challenging the expected, all in the name of possibility. We are neighbors caring for neighbors, working together as partners in health to improve the lives of the people we serve. If you share our passion for the health of our communities, advance your career with Nuvance Health! Additional Salary Detail The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity). Share: Apply Now Similar Jobs We are an equal opportunity employer Qualified applicants are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or any other classification protected under applicable Federal, State or Local law. We will endeavor to make a reasonable accommodation to the known physical or mental limitations of a qualified applicant with a disability unless the accommodation would impose an undue hardship on the operation or our business. 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