Clinical Research Associate
60K–80K a year
Behavioral Health Market Context
Apply Nowvia Learn4Good
Benefits
Dental CoverageHealth Insurance
Job Description
grity.
Key Responsibilities:
• Review and provide input on clinical study protocols, informed consent forms, and clinical study reports.
• Conduct site qualification, initiation, monitoring, and close-out visits in compliance with GCP, regulatory requirements, and SOPs.
• Collaborate with cross-functional teams (Data Management, Regulatory Affairs, and Clinical Operations) to develop data collection tools and ensure accurate data capture.
• Track and manage study documentation, including regulatory binders, site files, and ethics submissions.
• Ensure timely collection and review of essential documents and compliance with regulatory timelines.
• Identify and resolve site issues and protocol deviations, escalating as necessary.
• Assist in organizing investigator meetings and contribute to training materials and site support documentation.
• Maintain up-to-date knowledge of therapeutic areas, regulatory guidelines, and clinical trial processes.
Qualifications:
• Bachelor’s degree in a life science or healthcare-related field; advanced degree preferred.
• Minimum of 2 years of experience in clinical trial monitoring or clinical operations.
• Strong understanding of ICH-GCP guidelines and regulatory requirements.
• Excellent communication, organizational, and problem-solving skills.
• Ability to travel as needed to support clinical trial sites
Seniority level
• Seniority level Associate
Employment type
• Employment type
Contract
Job function
• Job function Research
• Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Meet Life Sciences by 2x
Inferred from the description for this job
Medical insurance
Vision insurance
401(k)
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Key Responsibilities:
• Review and provide input on clinical study protocols, informed consent forms, and clinical study reports.
• Conduct site qualification, initiation, monitoring, and close-out visits in compliance with GCP, regulatory requirements, and SOPs.
• Collaborate with cross-functional teams (Data Management, Regulatory Affairs, and Clinical Operations) to develop data collection tools and ensure accurate data capture.
• Track and manage study documentation, including regulatory binders, site files, and ethics submissions.
• Ensure timely collection and review of essential documents and compliance with regulatory timelines.
• Identify and resolve site issues and protocol deviations, escalating as necessary.
• Assist in organizing investigator meetings and contribute to training materials and site support documentation.
• Maintain up-to-date knowledge of therapeutic areas, regulatory guidelines, and clinical trial processes.
Qualifications:
• Bachelor’s degree in a life science or healthcare-related field; advanced degree preferred.
• Minimum of 2 years of experience in clinical trial monitoring or clinical operations.
• Strong understanding of ICH-GCP guidelines and regulatory requirements.
• Excellent communication, organizational, and problem-solving skills.
• Ability to travel as needed to support clinical trial sites
Seniority level
• Seniority level Associate
Employment type
• Employment type
Contract
Job function
• Job function Research
• Industries Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at Meet Life Sciences by 2x
Inferred from the description for this job
Medical insurance
Vision insurance
401(k)
Get notified when a new job is posted.
Sign in to set job alerts for “Clinical Research Associate” roles.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Qualifications
- •Minimum of 2 years of experience in clinical trial monitoring or clinical operations
- •Strong understanding of ICH-GCP guidelines and regulatory requirements
- •Excellent communication, organizational, and problem-solving skills
- •Ability to travel as needed to support clinical trial sites
Benefits
- •Medical insurance
- •Vision insurance
- •401(k)
Responsibilities
- •We are seeking a detail-oriented and proactive Clinical Research Associate to support the planning, execution, and monitoring of clinical trials
- •This role ensures compliance with regulatory requirements and company standards while contributing to high-quality data collection and study integrity
- •Review and provide input on clinical study protocols, informed consent forms, and clinical study reports
- •Conduct site qualification, initiation, monitoring, and close-out visits in compliance with GCP, regulatory requirements, and SOPs
- •Collaborate with cross-functional teams (Data Management, Regulatory Affairs, and Clinical Operations) to develop data collection tools and ensure accurate data capture
- •Track and manage study documentation, including regulatory binders, site files, and ethics submissions
- •Ensure timely collection and review of essential documents and compliance with regulatory timelines
- •Identify and resolve site issues and protocol deviations, escalating as necessary
- •Assist in organizing investigator meetings and contribute to training materials and site support documentation
- •Maintain up-to-date knowledge of therapeutic areas, regulatory guidelines, and clinical trial processes
- •Industries Pharmaceutical Manufacturing
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