Clinical Research Coordinator (Onsite)

Location: Dallas
Posted on: June 23, 2025

Job Description:

Shift : M-F 7am to 4pm hours may be adjusted by Hiring Division Director Research Coordinator Position Summary: The Research Coordinator supports and coordinates multiple clinical research protocols, acting as a liaison between site personnel, investigators, and sponsors. Under direct supervision, the coordinator will progressively gain expertise in clinical research operations, regulations, and human subject protection. Key Responsibilities: Coordinate operational activities for multiple research studies from feasibility to closeout. Serve as a primary contact between research staff, sponsors, and supervisors. Collaborate with site departments including finance, IRB, and hospital administration. Review study protocols with physicians and patients to ensure eligibility compliance. Ensure informed consent procedures and adherence to protocol requirements. Enter, verify, and manage data in Case Report Forms (CRFs) and electronic data systems. Create study-specific source documentation tools when not provided. Monitor for and report adverse events, protocol deviations, and violations. Track study supplies, including drug and device shipments. Respond to audits and monitoring visits. Attend site meetings, sponsor calls, investigator meetings, and training sessions. Education & Experience: Required: Bachelor's degree and 1 year of relevant experience (or equivalent education/experience) Preferred: Certified Clinical Research Coordinator (CCRC) Knowledge, Skills & Abilities: Knowledge: Familiarity with ICH-GCP, CFR regulations, and clinical research practices Understanding of medical terminology and site SOPs Skills: Strong organizational, communication, and time management skills Proficiency in basic clinical trial procedures (e.g., ECG, phlebotomy, specimen processing) Abilities: Attention to detail, self-motivation, and effective interpersonal interaction Ability to manage multiple studies with accuracy and compliance Clinical Competencies: May require annual demonstration of core clinical skills, including specimen handling and ECGs. Training and certification provided as needed per protocol. Travel Requirement: No Travel Occasional Travel (up to 25%) 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.

Keywords: , Keller , Clinical Research Coordinator (Onsite), Science, Research & Development , Dallas, Texas