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Clinical Research Coordinator
Benefits:
- Health insurance
- Opportunity for advancement
- Paid time off
- Training & development
Employment Type: Full‑time
Experience Required: 1+ year independently managing clinical studies (Required)
Languages: Fluent in English and Spanish (required)
About the Role
Experience Required: 1+ year independently managing clinical studies (Required)
Languages: Fluent in English and Spanish (required)
About the Role
We’re seeking a Bilingual Clinical Research Coordinator who can independently manage clinical studies from start to finish. This role is ideal for someone who has already served as the primary coordinator on their own protocols—handling regulatory tasks, participant coordination, data quality, and study operations with minimal oversight. You’ll work closely with investigators, sponsors, and participants to ensure studies run smoothly, ethically, and in full compliance with GCP and IRB requirements.
Key Responsibilities
- Serve as the primary coordinator for assigned clinical studies, managing all day‑to‑day operations.
- Conduct participant recruitment, screening, informed consent, and study visits in both English and Spanish.
- Maintain regulatory documentation, including IRB submissions, continuing reviews, amendments, and protocol deviations.
- Coordinate study start‑up activities, including site initiation, training, and logistics.
- Manage data entry, query resolution, and source documentation to ensure accuracy and audit readiness.
- Ensure compliance with GCP, FDA regulations, and institutional policies.
Required Qualifications
- Bilingual fluency in English and Spanish (verbal and written).
- 1+ year of experience independently coordinating clinical research studies, including direct responsibility for study visits and regulatory tasks.
- Strong understanding of GCP, human subjects' protection, and clinical research workflows.
- Proficiency with EMR systems, eCRFs, and common research platforms (e.g., CTMS tools).
Ability to work with diverse patient populations and maintain professionalism in sensitive situations.
Preferred Qualifications
- Experience with FDA‑regulated trials (drug or device).
- Certification such as CCRC, CCRA, or SOCRA/ACRP eligibility.
Phlebotomy skills or willingness to train.
What We Offer
Competitive compensation and benefits- Opportunities for professional development and certification
- The chance to contribute to studies that directly impact patient care and health outcomes
A collaborative, mission‑driven research environment
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