Clinical Research Coordinator I, Early Phase Clinical Research - Dallas, TX
About The Position
Join one of the world’s largest Clinical Research Organizations and support early-phase clinical trials in a fast‑paced, highly collaborative environment. As a Clinical Research Coordinator, you will oversee the operational execution of assigned studies, ensuring compliance with protocols, regulations, and SOPs while maintaining participant safety and data integrity. In this role, you’ll work closely with Project Managers, Principal Investigators, and site teams, serving as the primary site contact for study updates, issue escalation, and client requirements. You may also mentor junior staff and support moderately complex studies.
Requirements
- Bachelor’s degree in life sciences, pharmacy, or related field preferred; clinical/technical certifications accepted.
- 3+ years of experience in a clinical research or related environment (experience may substitute for education).
- Knowledge of study protocols, ICH/GCP guidelines, and the drug development process.
- Strong coordination, communication, and problem‑solving skills.
- Regular and consistent attendance.
Nice To Haves
- Customer service or team coordination experience preferred.
- Experience coordinating people or processes; customer‑service experience helpful.
Responsibilities
- Lead study start-up activities, including developing study-specific documents, schedules, and procedures.
- Coordinate key study events (check‑ins, PK days, check‑outs), ensuring participant safety, comfort, and protocol adherence.
- Attend and contribute to study meetings (e.g., Start-Up, Planning, Site Initiation).
- Review study protocols and provide site feedback on feasibility, logistics, and safety considerations.
- Partner with Operations, Pharmacy, and lab teams to ensure readiness, proper resourcing, and smooth dosing processes.
- Support client interactions, including visits, calls, and audits.
- Maintain accurate study documentation and oversee contributions to the eTMF.
- Identify and document protocol deviations and support quality improvement efforts.
- Complete other duties as assigned.
Benefits
- Medical
- Dental
- Vision
- Life
- STD/LTD (multiple insurance carriers)
- 401(K)
- Paid time off (PTO)
- Employee recognition awards
- Multiple ERG’s (employee resource groups)
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
