Biopharma Informatic · 1 day ago
Clinical Research Coordinator
Biopharma Informatic is seeking an experienced Spanish-speaking Clinical Research Coordinator to join their team. The role involves leading the coordination and execution of clinical trials, ensuring compliance with regulations, and serving as a liaison between physicians and study sponsors.
BiotechnologyClinical Trials
Responsibilities
Lead the coordination and execution of clinical trials across all phases: start-up, enrollment, maintenance, and close-out
Ensure proper receipt, handling, and accountability of investigational product (IP)
Conduct and document the informed consent process in compliance with protocols and regulations
Serve as a liaison between physicians, study sponsors, and internal team members
Achieve or exceed study enrollment targets at assigned sites
Complete accurate and timely data entry in electronic data capture systems
Resolve data queries promptly to support project timelines and database lock
Maintain compliance with GCP, company SOPs, and industry regulations
Qualification
Required
2–5 years of Clinical Research Coordinator experience in a physician practice or private research setting
Spanish Fluency - must be able to consent patient without translator
Phlebotomy experience is required
Strong understanding of investigational product (IP) receipt, handling, and accountability
Demonstrated ability to independently coordinate and manage clinical trials
Excellent organizational, communication, and problem-solving skills
Must be local to the area (onsite only; no relocation or remote work)
Preferred
Proven experience conducting the informed consent process