Clinical Research Coordinator

About this role

• **About the Role** We are looking for an experienced, bilingual Clinical Research Coordinator to help lead our clinical studies from start to finish.
• In this role, you will coordinate day-to-day study operations, safeguard participant safety and data integrity, and keep every protocol on track.
• You will be a central part of the team that makes our research succeed.
• **What You Will Do** * **Lead study execution:** Plan and coordinate clinical research projects, carry out key protocol events, and evaluate and analyze clinical data.
• * **Ensure compliance:** Monitor study activities for compliance with protocols, institutional policies, and local, state, and federal regulations.
• * **Recruit and enroll participants:** Screen potential participants through interviews, medical record reviews, and discussions with physicians and nurses, and oversee enrollment to ensure informed consent is properly obtained and documented.
• * **Support participants:** Oversee participant care during study visits, track enrollment status, and document withdrawals, including reasons and contact efforts.
• * **Monitor safety:** Record adverse events and side effects, and work with investigators to report them to the appropriate oversight agencies.
• * **Manage documentation:** Maintain accurate study records, including case report forms, drug dispensation logs, and regulatory documents.
• Audit participant files and resolve missing information or signatures.
• * **Prepare study materials:** Prepare protocol worksheets, procedure manuals, adverse event reports, and progress reports.
• * **Review and improve protocols:** Review proposed protocols for sample collection, data management, and participant risk.
• Identify protocol issues, alert investigators, and help resolve them, including through protocol revisions.
• * **Support audits:** Prepare for and participate in quality assurance audits by sponsors, federal agencies, and designated review groups.
• * **Train the team:** Train staff on the scientific and procedural aspects of studies, including standards of care, informed consent, and documentation.
• * **Handle specimens and lab support:** Collect and process specimens according to established policies, and serve as backup for laboratory and other functions as needed.
• * **Coordinate supplies and logistics:** Order and receive study drugs and devices as needed, support study technology and equipment, and manage administrative items such as participant compensation.
• * **Contribute beyond the study:** Complete special projects such as surveys, statistical reports, and research studies, contribute to broader center needs, and take on other duties assigned by the Administrator or Clinic Director.
• **What You Bring** * Bachelor's degree in life sciences or a related field (master's degree preferred) * 3 to 5 years of clinical research or related experience * Fluency in Spanish and English * Strong knowledge of biological and medical terminology * Exceptional organization and attention to detail * Excellent communication and interpersonal skills * Solid understanding of administrative and management principles * Comfort using study technology, including ePRO tablets and other electronic devices **Physical Requirements** * Ability to sit for extended periods at a desk and computer, and to stand for extended periods in a laboratory * Ability to occasionally lift up to 15 pounds **Compensation, Benefits, and Schedule** **Pay:** $20.00 - $23.00/ hour **Benefits:** 100% employer-paid health insurance **Schedule:** Monday through Friday, 7:00 a.m.
• to 4:00 p.m.C

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