Clinical Research Site Manager
Behavioral Health Market Context
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Job Description
erformance, and maintaining the highest standards of ethics, safety, and data integrity.
Role Overview
We are seeking an experienced Clinical Research Site Manager to oversee daily operations across one or more research sites.
This role is responsible for ensuring protocol compliance, operational efficiency, and high-quality study execution , while leading site teams and supporting patient recruitment and retention efforts.
On Site in Plano, TX but able to travel to all sites in the DFW area and Austin, as necessary.
KEY RESPONSIBILITIES
• Oversee day-to-day clinical trial operations at assigned site(s)
• Ensure compliance with study protocols, GCP, FDA, and IRB requirements
• Manage site staff, including CRCs, research assistants, and support teams
• Coordinate with physicians, nurses, sponsors, and CROs
• Drive patient recruitment, enrollment, and retention strategies
• Maintain accurate and timely source documentation and data integrity
• Monitor study timelines, milestones, and performance metrics
• Prepare for and support monitoring visits, audits, and inspections
• Identify and resolve operational challenges to ensure study success
QUALIFICATIONS
• Prior experience managing 2 or more clinical research sites required
• Strong experience in clinical trials, protocol execution, and clinical operations
• Proven project management and leadership skills
• Excellent organizational, communication, and problem-solving abilities
• Ability to work effectively in a fast-paced, multi-site environment
• Experience in clinical research or healthcare required
• Bachelors degree required; advanced degree preferred
Applicants must be authorized to work in the United States for any employer. We are not able to sponsor employment visas at this time.
Role Overview
We are seeking an experienced Clinical Research Site Manager to oversee daily operations across one or more research sites.
This role is responsible for ensuring protocol compliance, operational efficiency, and high-quality study execution , while leading site teams and supporting patient recruitment and retention efforts.
On Site in Plano, TX but able to travel to all sites in the DFW area and Austin, as necessary.
KEY RESPONSIBILITIES
• Oversee day-to-day clinical trial operations at assigned site(s)
• Ensure compliance with study protocols, GCP, FDA, and IRB requirements
• Manage site staff, including CRCs, research assistants, and support teams
• Coordinate with physicians, nurses, sponsors, and CROs
• Drive patient recruitment, enrollment, and retention strategies
• Maintain accurate and timely source documentation and data integrity
• Monitor study timelines, milestones, and performance metrics
• Prepare for and support monitoring visits, audits, and inspections
• Identify and resolve operational challenges to ensure study success
QUALIFICATIONS
• Prior experience managing 2 or more clinical research sites required
• Strong experience in clinical trials, protocol execution, and clinical operations
• Proven project management and leadership skills
• Excellent organizational, communication, and problem-solving abilities
• Ability to work effectively in a fast-paced, multi-site environment
• Experience in clinical research or healthcare required
• Bachelors degree required; advanced degree preferred
Applicants must be authorized to work in the United States for any employer. We are not able to sponsor employment visas at this time.
Qualifications
- •Prior experience managing 2 or more clinical research sites required
- •Strong experience in clinical trials, protocol execution, and clinical operations
- •Proven project management and leadership skills
- •Excellent organizational, communication, and problem-solving abilities
- •Ability to work effectively in a fast-paced, multi-site environment
- •Experience in clinical research or healthcare required
- •Applicants must be authorized to work in the United States for any employer
Benefits
Responsibilities
- •We are seeking an experienced Clinical Research Site Manager to oversee daily operations across one or more research sites
- •This role is responsible for ensuring protocol compliance, operational efficiency, and high-quality study execution , while leading site teams and supporting patient recruitment and retention efforts
- •On Site in Plano, TX but able to travel to all sites in the DFW area and Austin, as necessary
- •Oversee day-to-day clinical trial operations at assigned site(s)
- •Ensure compliance with study protocols, GCP, FDA, and IRB requirements
- •Manage site staff, including CRCs, research assistants, and support teams
- •Coordinate with physicians, nurses, sponsors, and CROs
- •Drive patient recruitment, enrollment, and retention strategies
- •Maintain accurate and timely source documentation and data integrity
- •Monitor study timelines, milestones, and performance metrics
- •Prepare for and support monitoring visits, audits, and inspections
- •Identify and resolve operational challenges to ensure study success
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