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Clinical Research Operations Manager Jobs (NOW HIRING)

TriHealth

Manager Clinical Research

Montgomery, OH · On-site

In this role, you'll oversee research operations from - program development and regulatory ... The Manager of Clinical Research is responsible for establishing and maintaining a Research Program ...

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

As of May 30, 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.

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.

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.
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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 May 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 Director

Serv Recruitment Agency

Albuquerque, NM • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 16 days ago

Job description

Join the Southwest Women's Oncology Team:

Southwest Women's Oncology Team (SWWO) is rapidly growing and looking for a dedicated and driven Clinical Research Director to join their high-performance team. SWWO's integrated group of healthcare professionals provides expert, compassionate care and delivers curative outcomes for their patients. With a focus on advanced surgical techniques, clinical trials, and patient advocacy, SWWO is uniquely positioned as a private practice with state-of-the-art resources and strong institutional partnerships.

This Role includes:
  • Build, scale, and manage the clinical research vertical within SWWO, developing long-term strategy, infrastructure, and resourcing plans.
  • Partner with the Executive Team to align research strategy with organizational goals.
  • Evaluate new research opportunities and develop business cases for study selection, site expansion, and partnerships.
  • Lead the full lifecycle of clinical trials, including feasibility, start-up, recruitment, execution, monitoring, and close-out.
  • Oversee study budgets, billing compliance, and financial performance; ensure accurate reporting and forecasting.
  • Maintain compliance with ICH-GCP, FDA, NIH, and institutional requirements.
  • Develop, implement, and maintain Standard Operating Procedures (SOPs) for research operations.
  • Manage, mentor, and develop a team of Clinical Research Coordinators (CRCs), Data Specialists, and support staff.
  • Create a culture of excellence, accountability, and continuous improvement.
  • Oversee hiring, onboarding, training, and performance management for the research team.
  • Serve as primary liaison for sponsors, CROs, investigators, and regulatory agencies.
  • Support Principal Investigators in protocol execution and ensure appropriate documentation and data integrity.
  • Represent SWWO in research networks, professional associations, and at industry conferences.
  • Ensure all research is conducted ethically and adheres to institutional, state, and federal regulations.
  • Oversee audit readiness and corrective action processes.
  • Identify and implement process improvements and new technologies to optimize research operations.
Qualifications:
  • Strong leadership skills with the ability to effectively communicate and create a high-performance environment.
  • Proven leadership experience in clinical research within oncology or a complex medical setting.
  • Demonstrated ability to build, scale, and manage a research program or site.
  • Strong business and financial acumen; experience with clinical research budgeting, billing, and contracts.
  • Excellent communication, relationship management, and negotiation skills.
  • Deep understanding of GCP, FDA, and clinical research compliance standards.
  • Ability to coordinate therapeutic phase II-IV drug or device trials.
  • Be adaptable, flexible, and able to change as required.

Education and Experience:

  • Bachelor's degree in a health science, life science, or related field required; Master's degree preferred.
  • 10+ years of clinical research experience, including 5+ years in a leadership or director-level role.
  • Certification (CCRP, CCRC, or equivalent) strongly preferred.
  • Prior experience leading oncology clinical trials highly desirable.
Physical Requirements:
  • Prolonged periods of sitting and working on a computer.
  • Ability to lift up to 15 pounds as needed.
Our Dream Teammate will have access to:
  • Competitive Salary
  • Excellent Benefits: Medical, dental, vision, PTO, and 401K
  • High-Performance Concierge Culture
  • Performance Center: Full AI gym suite, recovery modalities, group fitness classes, body composition tracking, and state-of-the-art aesthetic modalities.

Job Type: Full-time
Location: Albuquerque, New Mexico