Clinical Research Coordinator
Behavioral Health Market Context
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Job Description
l research more efficient and accessible. They focus on on large-volume recruitment and retention of diverse and specialty patient populations, and have an experienced team with extensive physician partnerships help deliver high-quality data across a wide range of therapeutic areas!
The Role:
We are seeking an temporary CRC to support the site for 3 - 4 months. There is eligibility for a permanent role based on site needs and performance
• Coordinate all aspects of assigned clinical trials
• Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards
• Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
• Manage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)
• Ensure timely EDC data entry and resolution of queries
• Report and follow up on AEs, SAEs, and protocol deviations
• Collaborate with investigators, sponsors/CROs, labs, and internal teams
• Prepare for and participate in monitoring visits, audits, and inspections
• Maintain regulatory documentation and ensure training compliance for amendments and systems
• Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
• Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
Requirements:
• 1+ years exp as a Research Assistant or CRC on sponsor backed trials
• Ability to work on site M-F (NO hybrid or remote days)
• Ok with a 3 month employment term to start
The Role:
We are seeking an temporary CRC to support the site for 3 - 4 months. There is eligibility for a permanent role based on site needs and performance
• Coordinate all aspects of assigned clinical trials
• Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards
• Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
• Manage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)
• Ensure timely EDC data entry and resolution of queries
• Report and follow up on AEs, SAEs, and protocol deviations
• Collaborate with investigators, sponsors/CROs, labs, and internal teams
• Prepare for and participate in monitoring visits, audits, and inspections
• Maintain regulatory documentation and ensure training compliance for amendments and systems
• Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
• Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
Requirements:
• 1+ years exp as a Research Assistant or CRC on sponsor backed trials
• Ability to work on site M-F (NO hybrid or remote days)
• Ok with a 3 month employment term to start
Qualifications
- •Studies in allergy, asthma, vaccines, and more!
- •Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory
- •1+ years exp as a Research Assistant or CRC on sponsor backed trials
- •Ability to work on site M-F (NO hybrid or remote days)
- •Ok with a 3 month employment term to start
Benefits
- •3 Month Employment (W2), with possibility for permanent after 3 months
- •$35 - $45/hr for 3 month contract terms
- •Mon - Fri Schedule; fully on on site
Responsibilities
- •We are seeking an temporary CRC to support the site for 3 - 4 months
- •There is eligibility for a permanent role based on site needs and performance
- •Coordinate all aspects of assigned clinical trials
- •Conduct subject visits and ensure accurate, timely documentation in compliance with all applicable standards
- •Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
- •Manage subject recruitment, informed consent, and retention activities (There is a recruitment team to support day to day recruitment)
- •Ensure timely EDC data entry and resolution of queries
- •Report and follow up on AEs, SAEs, and protocol deviations
- •Collaborate with investigators, sponsors/CROs, labs, and internal teams
- •Prepare for and participate in monitoring visits, audits, and inspections
- •Maintain regulatory documentation and ensure training compliance for amendments and systems
- •Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)