Job Description

Shift : M-F 7am to 4pm hours may be adjusted by Hiring Division Director Position Summary: The Research Coordinator is responsible for managing multiple clinical research protocols and acting as a liaison between investigators, sponsors, and internal teams. Under direct supervision, this role supports research operations and regulatory compliance while gaining foundational knowledge in human subject research. Key Responsibilities: Adhere to the organization's Code of Conduct and Mission & Values. Complete all assigned training by designated deadlines. Support the operational activities of multiple ongoing research protocols. Serve as a liaison among site personnel, industry sponsors, and supervisors. Coordinate with departments including finance, hospital administration, and IRBs. Oversee assessment schedules from feasibility submission through study closeout. Review study design and inclusion/exclusion criteria with physicians and participants. Ensure patient protection and protocol compliance during informed consent processes. Review and maintain data accuracy through source document verification. Create study-specific source documentation tools when necessary. Enter and manage data in case report forms or electronic data capture systems. Track shipments of drugs, devices, and study supplies. Monitor and report adverse events, protocol deviations, and violations. Communicate study-related concerns to supervisors or designated personnel. Participate in study meetings, audits, and sponsor visits as required. Review and respond to findings from monitoring and auditing activities. Education & Experience: Required: Bachelor's degree 1 years of relevant clinical research experience or equivalent education/experience Preferred: Degree in healthcare, science, or a related field Certified Clinical Research Coordinator (CCRC) Knowledge, Skills & Abilities: Knowledge: Familiarity with organizational SOPs and clinical research systems Emerging understanding of ICH guidelines and FDA regulations Basic knowledge of medical terminology Skills: Strong communication and time management Proficient in data accuracy and documentation Basic clinical procedures (e.g., ECGs, phlebotomy, specimen handling/shipping) Abilities: Strong interpersonal and collaborative skills Self-motivated with high attention to detail Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services. Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Nesco Resource

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