Bilingual Research Coordinator
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
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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