Biopharma Informatic · 2 hours ago
Clinical Research Coordinator
McAllen, TX
Full-time
Onsite
Entry, Mid Level
2+ years expBiopharma Informatic is seeking an experienced Clinical Research Coordinator (CRC) to join our team. The role involves leading the coordination and execution of clinical trials, ensuring compliance with protocols, and serving as a liaison among various stakeholders.
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
Strong understanding of investigational product (IP) receipt, handling, and accountability
Proven experience conducting the informed consent process
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)
Company
Biopharma Informatic
Biopharma Informatic is a clinical research company that provides clinical trials and prepares documentation on different protocols.
51-200 employees
Funding
Current Stage
Growth StageLeadership Team
Shuja Naqvi
Chief Executive Officer
Company data provided by crunchbase