Full-Time Research Coordinator
Redondo Beach, CAFull-time
25–35 an hour
Behavioral Health Market Context
Apply Nowvia VPPPA Job Board
Benefits
Dental CoverageHealth Insurance
Job Description
certification and compliance, subject recruitment, conducting study specific tasks and assessments and adequate enrollment for multiple clinical trials.
Must show strong administrative and time management skills for clinical research.
Previous research experience is desired but not necessary.
Required Qualifications
· Ability to obtain required certifications (GCP, IATA, etc.)
· Must posses the inter personal skills needed to maintain patient retention during all studies.
· Time management skills to coordinate multiple clinical trials simultaneously and conduct multiple patient visits and screenings daily.
Job Duties
• Performing complex subject visits
• Electronic data collection (EDC) programs and ability to complete data entry in a timely manner
• Navigating Institutional Review Board (IRB) submissions, continuing reviews and reports.
• Working with multiple Clinical Research Associates (CRA) to conduct onsite and virtual monitoring visits.
• Project and clinical trial experience including regulatory and compliance responsibilities.
• Source document generation
• Maintaining FDA documentation and regulatory documents
Preferred Qualifications
· Phlebotomy license preferred.
Full Time, Non-Exempt.
• Benefits: Medical, Vision,401K,Paid Holidays, Staff Discounts
Job Type: Full-time
Pay: $25.00 - $35.00 per hour
Benefits:
• 401(k)
• 401(k) matching
• Employee discount
• Flexible spending account
• Health insurance
• Vision insurance
Application Question(s):
• How many years of experience do you have with clinical research/trials?
• Have you used electronic data collection programs?
• Do you have a phlebotomy license?
Education:
• Bachelor's (Preferred)
Work Location: In person
Must show strong administrative and time management skills for clinical research.
Previous research experience is desired but not necessary.
Required Qualifications
· Ability to obtain required certifications (GCP, IATA, etc.)
· Must posses the inter personal skills needed to maintain patient retention during all studies.
· Time management skills to coordinate multiple clinical trials simultaneously and conduct multiple patient visits and screenings daily.
Job Duties
• Performing complex subject visits
• Electronic data collection (EDC) programs and ability to complete data entry in a timely manner
• Navigating Institutional Review Board (IRB) submissions, continuing reviews and reports.
• Working with multiple Clinical Research Associates (CRA) to conduct onsite and virtual monitoring visits.
• Project and clinical trial experience including regulatory and compliance responsibilities.
• Source document generation
• Maintaining FDA documentation and regulatory documents
Preferred Qualifications
· Phlebotomy license preferred.
Full Time, Non-Exempt.
• Benefits: Medical, Vision,401K,Paid Holidays, Staff Discounts
Job Type: Full-time
Pay: $25.00 - $35.00 per hour
Benefits:
• 401(k)
• 401(k) matching
• Employee discount
• Flexible spending account
• Health insurance
• Vision insurance
Application Question(s):
• How many years of experience do you have with clinical research/trials?
• Have you used electronic data collection programs?
• Do you have a phlebotomy license?
Education:
• Bachelor's (Preferred)
Work Location: In person
Qualifications
- •Ability to obtain required certifications (GCP, IATA, etc.)
- •Must posses the inter personal skills needed to maintain patient retention during all studies
- •Time management skills to coordinate multiple clinical trials simultaneously and conduct multiple patient visits and screenings daily
Benefits
- •Full Time, Non-Exempt
- •Benefits: Medical, Vision,401K,Paid Holidays, Staff Discounts
- •Pay: $25.00 - $35.00 per hour
- •401(k)
- •401(k) matching
- •Employee discount
- •Flexible spending account
- •Health insurance
- •Vision insurance
Responsibilities
- •The position is responsible for conducting multiple FDA clinical trials alongside other clinical research coordinators
- •This role will be a direct report to the lead clinical research coordinator
- •Reporting to the Principal Investigator (PI) and lead clinical research coordinator (CRC), the individual will have central responsibility for ensuring GCP certification and compliance, subject recruitment, conducting study specific tasks and assessments and adequate enrollment for multiple clinical trials
- •Must show strong administrative and time management skills for clinical research
- •Performing complex subject visits
- •Electronic data collection (EDC) programs and ability to complete data entry in a timely manner
- •Navigating Institutional Review Board (IRB) submissions, continuing reviews and reports
- •Working with multiple Clinical Research Associates (CRA) to conduct onsite and virtual monitoring visits
- •Project and clinical trial experience including regulatory and compliance responsibilities
- •Source document generation
- •Maintaining FDA documentation and regulatory documents
More Jobs
- Entry Level Clinical Research Roleat Care Health
- Autism ABA Behavior Technician 1:1 Therapy & Dataat Star ABA
- Entry-Level Clinical Research Side Incomeat Care Health
- Entry-Level Clinical Research Side Incomeat Care Health
- Behavioral Health Community Liaisonat Aviation ABA Therapy
- Psychedelic ARNPat Segal Institute for Clinical Research
- Operations Team Lead – Clinical Researchat Om Research LLC
- OPS - Clinical Research Coordinatorat University of Florida
- Entry-Level Clinical Research Side Incomeat Care Health
- BCBA: Lead Therapy, Mentorship & Growth Pathat Action Behavior Centers