We are looking for a well versed Clinical Research Coordinator that is bilingual/fluent in Spanish. The ideal candidate will have a minimum of 2 years of experience as a CRC and have experience with tasks such as EKGs, vitals, & phlebotomy. This position is on-site and a direct hire (permanent).

Responsibilities

• Perform overall data management of studies - collect, enter, and maintain records for clinical study subjects.
• Support accurate and timely data entry in electronic databases.
• Ensure all protocol-required procedures and visits occur according to specified guidelines.
• Manage participant enrollment and ensure compliance with the protocol during participant recruitment, informed consent, participant education, eligibility assessment, participant care, and follow-up per protocol.
• Collaborates with quality assurance (QA) in the development of source documentation for new studies, assisting in the assessment of toxicities/adverse events and reporting serious adverse events per IRB and sponsor requirements.
• Possess excellent interpersonal skills and collaborative with the research team.
• Independently manage workflows and prioritize numerous tasks.
• Be flexible and anticipate timeframes to accommodate frames subjects, monitors, and overtime hours during high-enrolling study periods.
• Maintains GCP certification and IATA training as required.
• Performs other duties as assigned.

Requirements

• At least two years of experience as a clinical research coordinator.
• Experience with Phlebotomy
• Excellent oral and written communication skills.
• Demonstrated ability to work well independently and with subordinates.
• Demonstrated ability to manage frequent deadlines and competing priorities.
• Computer proficiency.
• Critical thinking and analytical skills