Job Description

Job Description:

Biopharma Informatic is seeking an experienced Clinical Research Coordinator (CRC) to join our team. This is a fully onsite role and is open only to candidates who are local to the area.

We are specifically looking for individuals with hands-on Clinical Research Coordinator experience in physician office or private practice clinical trial settings. Experience gained exclusively in hospital or university-based research environments does not fully align with the workflow and operational structure of this position.

Required Spanish Fluency - Important Notice:

Due to the needs of our patient population and the communication demands of this role, Spanish fluency is a strict requirement for this position. Unfortunately, we cannot consider applicants who are not fluent in Spanish, regardless of other qualifications or experience.

If you are not a Spanish speaker but are interested in joining Biopharma Informatic, we encourage you to explore and apply to any of our other open positions that align with your background. Please submit your application anytime through our careers portal: 🔗

Key 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.

Qualifications:

• 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).

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