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Clinical Research Operations Manager Jobs (NOW HIRING)

Denali Health

Clinical Operations Manager

Atlanta, GA · On-site

Denali Health is a fast-growing clinical research organization focused on accelerating therapies to market through operational excellence, exceptional talent, and a participant-centered approach to ...

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How much do clinical research operations manager jobs pay per year?

As of Jul 7, 2026, the average yearly pay for clinical research operations manager in the United States is $98,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $113,500.00 per year, depending on experience, location, and employer.

How does a Clinical Research Operations Manager collaborate with cross-functional teams during a study?

As a Clinical Research Operations Manager, you will work closely with cross-functional teams including clinical trial coordinators, data managers, regulatory affairs specialists, and principal investigators. Your role involves facilitating clear communication between departments, ensuring that study milestones are met, and resolving operational issues as they arise. Regular meetings and status updates are common, and you'll often act as a liaison to keep all stakeholders aligned on study objectives, timelines, and compliance requirements. This collaborative approach is crucial for maintaining study integrity and ensuring successful trial outcomes.

What does a Clinical Research Operations Manager do?

A Clinical Research Operations Manager oversees the daily operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. They coordinate between research staff, sponsors, and regulatory bodies, manage budgets and timelines, and ensure proper documentation and reporting. Their role is essential in maintaining the quality and integrity of clinical studies from start to finish.

What are the key skills and qualifications needed to thrive as a Clinical Research Operations Manager, and why are they important?

To thrive as a Clinical Research Operations Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications such as ACRP or SOCRA are highly valuable. Leadership, problem-solving, and excellent organizational and communication skills help you manage teams and collaborate effectively with stakeholders. These skills and qualities are crucial for ensuring the successful execution of clinical trials while maintaining regulatory standards and operational efficiency.
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Clinical Research Operations Manager jobs near you
Infographic showing various Clinical Research Operations Manager job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $98,039 per year, or $47.1 per hour.

Clinical Research Operations Manager

SRA Trials

Miami, FL

$75K - $90K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted yesterday

Job description

Skills: Clinical Research Operations Manager
We seek a highly motivated and experienced Clinical Research Operations Manager to join our team. The successful candidate will oversee the day-to-day operations of clinical research studies, ensure compliance with regulatory requirements, and manage study timelines and budgets.
Responsibilities:
  • Manage the planning, execution, and monitoring of clinical research studies
  • Ensure compliance with regulatory requirements and ethical standards
  • Collaborate with cross-functional teams to ensure successful study execution
  • Manage study vendors and contractors
  • Provide regular updates to senior management on study progress and issues
  • Identify and mitigate study risks
  • Ensure data quality and integrity
  • Work closely with the Clinical Operations Director, Site Director, and Principal Investigators to coordinate all research activities on-site while ensuring protocol adherence and patient safety
  • Serve and assist as the liaison between the Site and the Sponsor and FDA representatives
  • Ability to multi-task and manage several projects in parallel, paying attention to detail
  • Ensure that all clinical research duties are performed according to protocols, sponsor's guidelines, GCP amp; ICH guidelines, as well as local and FDA regulations
  • Assist with Hiring and training all clinical department staff
  • Team building and conflict resolution within the clinical team
  • Assist the Clinical Operations Director in the process of seeking, vetting, managing, and training all vendors associated with the site
  • Identify project issues such as resource, technical, or scheduling constraints, and assist in resolving issues internally and externally by performing risk assessments and developing summarized options and proposed solutions
  • Ensure that projects are completed on time, within budget and scope, and conform to pre-established quality standards
  • Primary contact to all the IRBs, CROs, Sponsors, and Study Vendors
  • Assist during Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close Out Visits
  • Assist during Sponsor Audits and FDA Inspections
  • Create GCP-compliant source documents and review all documents related to clinical trials
  • Collect and distribute site metrics for internal departmental meetings and the site's Business Development department
  • CTMS training and implementation
  • Management of site calendar
  • Organizes and manages internal team meetings, investigator meetings, and other trial-specific meetings
Requirements:
  • Bachelor's degree in a scientific or healthcare-related field
  • Minimum of 5 years of experience in clinical research operations management
  • Strong knowledge of FDA regulations and ICH guidelines
  • Excellent project management skills
  • Strong communication and interpersonal skills
  • Ability to work independently and as part of a team
  • Strong problem-solving and decision-making skills
  • Proficiency in Microsoft Office and clinical trial management systems

Job Type: Full-time

Benefits:

  • Dental Insurance
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Vision insurance

Schedule:

  • 8-hour shift
  • Monday to Friday
  • Weekend availability

Ability to commute/relocate:

  • Miami, FL 33172: Reliably commute or planning to relocate before starting work (Required)

Work Location: In person

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