Bilingual Research Coordinator

The Neuron Clinic Gp

Chula Vista, CAFull-timePosted Mar 31, 2026

25–30 an hour

Behavioral Health Market Context

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Benefits

Health InsurancePaid Time Off

Job Description

ation of clinical research trials protocols, and supports interactions with CROs/CRAs, and trial participants.

The ideal candidate will have research experience at the site level.

Other Requirements: Able to work out of the San Marcos location, sometimes travel to Chula Vista location.

Essential Duties and Responsibilities
• Coordinates implementation of trial protocol.
• Ensures complete and proper execution of the protocol schedule of assessments.
• Assist in participants recruiting using proper regulatory approved documents, and recruitment procedures.
• Prepares review of inclusion/exclusion criteria for participant eligibility, per protocol.
• Schedules prescreening, and screening activities.
• Maintains current potential participants list in accordance to OHRPP, IRB, ICH/GCP, and other applicable regulations.
• Tracks participants' progress in the study, prepares and manages participant study binders, following proper completion of source document worksheets, and makes sure PI/Sub-I complete their tasks for each visit.
• Participates in monitoring visits.

Preferred Education and Experience
• Bachelors or other college degree preferred
• Experience in cognitive testing preferred
• Blood collection and processing preferred
• Phlebotomy certification preferred.
• CITI certification preferred
• Good Clinical Practice (GCP).
• Human Research Protection Program (HRPP).

Knowledge Skills and Abilities
• Self-motivated and desire to learn and grow in healthcare
• Strong attention to detail
• Excellent analytical and critical thinking skills
• Excellent verbal and written communication skills and the ability to communicate effectively with patients, providers and payors
• The ability to prioritize and multitask efficiently and effectively
• Strong commitment to actively supporting an ethical working environment
• Strong knowledge of computer-based systems such as Excel, Word, and the Internet with the ability to quickly learn new systems.
• Bilingual English/Spanish
Schedule
• 8 hour shift
• Monday - Friday
Special Conditions of Employment
• Furnish proof of COVID-19 vaccination

Qualifications

  • The ideal candidate will have research experience at the site level
  • Other Requirements: Able to work out of the San Marcos location, sometimes travel to Chula Vista location
  • Self-motivated and desire to learn and grow in healthcare
  • Strong attention to detail
  • Excellent analytical and critical thinking skills
  • Excellent verbal and written communication skills and the ability to communicate effectively with patients, providers and payors
  • The ability to prioritize and multitask efficiently and effectively
  • Strong commitment to actively supporting an ethical working environment
  • Strong knowledge of computer-based systems such as Excel, Word, and the Internet with the ability to quickly learn new systems
  • Bilingual English/Spanish
  • Furnish proof of COVID-19 vaccination

Benefits

  • Health insurance
  • Paid time off
  • Training & development
  • 8 hour shift

Responsibilities

  • Research Coordinator assists investigators and coordinates proper implementation of clinical research trials protocols, and supports interactions with CROs/CRAs, and trial participants
  • Coordinates implementation of trial protocol
  • Ensures complete and proper execution of the protocol schedule of assessments
  • Assist in participants recruiting using proper regulatory approved documents, and recruitment procedures
  • Prepares review of inclusion/exclusion criteria for participant eligibility, per protocol
  • Schedules prescreening, and screening activities
  • Maintains current potential participants list in accordance to OHRPP, IRB, ICH/GCP, and other applicable regulations
  • Tracks participants' progress in the study, prepares and manages participant study binders, following proper completion of source document worksheets, and makes sure PI/Sub-I complete their tasks for each visit
  • Participates in monitoring visits


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