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Clinical Operations Jobs (NOW HIRING)

ALLIANCE CLINICAL LLC

Clinical Operations Manager

Houston, TX · On-site

$90K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Operations Manager is responsible for daily clinic operations, administrative functions, and the management of office personnel. This role acts as a liaison between patients, medical ...

ALLIANCE CLINICAL LLC

Clinical Operations Manager

Inglewood, CA · On-site

$120K - $148K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Operations Manager is responsible for daily clinic operations, administrative functions, and the management of office personnel. This role acts as a liaison between patients, medical ...

Clinovo

Dir, Clinical Operations

Cambridge, MA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The successful candidate will lead clinical operations for an autoimmune and immunology-focused development portfolio, with a particular emphasis on early-phase and operationally complex studies.

Whoop

Director, Clinical Operations

Boston, MA · On-site

As the Director, Clinical Operations, you will lead the clinical operations function responsible for executing the studies that support WHOOP's regulated and unregulated health features, with a ...

Icon plc

Manager Clinical Operations

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Manager, Clinical Operations ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

New

Iota Biosciences

Manager, Clinical Operations

Alameda, CA · On-site

$145K - $200K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Role We're seeking a Manager of Clinical Operations to lead the oversight, planning, coordination, and execution of clinical projects for our Class III active implantable device program. This ...

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Clinical Operations information

See salary details

$35K

$98K

$186.5K

How much do clinical operations jobs pay per year?

As of Aug 14, 2026, the average yearly pay for clinical operations 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 operations professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Operations professionals play a central role in coordinating activities among various teams such as regulatory affairs, data management, biostatistics, and clinical research associates. They ensure that timelines are met, protocols are followed, and all departments are aligned with trial objectives. Regular meetings, clear communication, and the ability to anticipate and resolve operational challenges are essential to successful collaboration. This cross-functional teamwork helps maintain trial quality and regulatory compliance throughout the study.

What is clinical operations?

Clinical operations refers to the planning, management, and execution of clinical trials and research studies within the healthcare and pharmaceutical industries. Professionals in clinical operations ensure that studies are conducted efficiently, ethically, and in compliance with regulatory requirements. Their responsibilities may include site management, patient recruitment, data collection, and ensuring protocol adherence. The goal is to facilitate the safe and effective development of new medical treatments and therapies.

What is the difference between Clinical Operations vs Clinical Research Associate?

AspectClinical OperationsClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trial managementBachelor's degree, often with certification in clinical research
Work EnvironmentProject management, coordinating multiple trial sitesMonitoring clinical sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies
Common Search & ComparisonFocuses on trial oversight and managementFocuses on site monitoring and data verification

Clinical Operations professionals oversee the planning, coordination, and management of clinical trials, ensuring they run smoothly across multiple sites. Clinical Research Associates primarily monitor clinical trial sites, verify data accuracy, and ensure compliance with protocols. While both roles require knowledge of clinical research, Clinical Operations has a broader scope involving project management, whereas CRAs focus on site-level monitoring.

What are the key skills and qualifications needed to thrive in clinical operations, and why are they important?

To thrive in Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and electronic data capture (EDC) platforms is essential. Strong leadership, problem-solving, and communication skills help coordinate teams and ensure project timelines are met. These skills are crucial for guaranteeing efficient, compliant, and successful clinical trial execution in a highly regulated environment.
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What are the most commonly searched types of Clinical Operations jobs?

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What states have the most Clinical Operations jobs?

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Clinical Operations jobs near you
Infographic showing various Clinical Operations job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $98,039 per year, or $47.1 per hour.

Clinical Operations Manager

Pinnacle Clinical Research

Austin, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New

Job description

Summary: The Clinical Operations Manager is responsible for operational implementation of assigned studies at their research site. The incumbent supervises clinical trial staff and works closely with the Principal Investigator, Site Director and Regional Director, and cross-functional teams to ensure successful completion of research activities. This role serves as the primary liaison between the research site, sponsors, CROs, and other stakeholders while maintaining compliance with regulations.
Duties and Responsibilities:
Clinical Trial Management
  • Oversee daily operations of clinical research staff and studies
  • Coordinate multiple projects with competing priorities and deadlines
  • Monitor adherence to protocols and study timelines
  • Act as primary liaison with sponsors, CROs, and vendors
  • Prepare for and facilitate study monitor visits
Regulatory Compliance
  • Ensure adherence to Standard Operating Procedures (SOPs), FDA regulations, and other regulatory references
  • Maintain subject and document confidentiality and privacy
  • Assist with regulatory submissions and file maintenance
  • Create and implement corrective and preventive action plans when appropriate
Study Documentation
  • Supervise creation and completion of study-related documents
  • Supervise completion of case report forms
  • Supervise documentation of adverse events and subject history
  • Prepare reports as requested
Study Participant Coordination
  • Supervise study assessments with study participants including informed consent
  • Supervise subject screening and recruitment
  • Supervise appointment scheduling and visit implementation
  • Supervise collection of vital signs and study participant assessments
  • Supervise phlebotomy, specimen processing, and biological sample shipping
Resource Management
  • Identify departmental needs for supplies, staffing, and equipment
  • Improve research processes within established guidelines
Supervisory Responsibilities: Directly supervises Clinical Research Coordinators and Research Assistants, ensuring compliance with SOPs and regulations. Carries out supervisory responsibilities according to organizational policies and applicable laws, including:
  • Training employees
  • Planning, assigning, and directing work (with management guidance)
  • Appraising performance
  • Addressing complaints and resolving problems
Education/Experience:
  • High school diploma or GED required; Bachelor's degree preferred
  • Three to five years of experience in a Clinical Research Coordinator role
  • Previous experience managing clinical research coordinators preferred
  • For CNS sites, experience conducting rating scales such as MMSE
Certificates and Licenses:
  • Good Clinical Practice training certification
  • IATA training certification
  • Valid driver's license and insurance
Knowledge, Skills, and Other Abilities:
  • Strong oral and written communication abilities
  • Excellent organizational skills and attention to detail
  • Professional interpersonal skills with a positive demeanor
  • Adaptability to changing priorities
  • Medical knowledge including terminology
  • Thorough understanding of regulations, regulatory guidance, and SOPs
  • Proficiency with Microsoft Office, web browsers, and electronic case report form systems
Work Environment and Physical demands:
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Office/laboratory and clinical environment.
  • Exposure to biological fluids and/or bloodborne pathogens.
  • Personal protective equipment required
  • Occasional domestic and international travel
  • Ability to maintain upright/stationary position for 6-10 hours daily
  • Frequent mobility required.
  • Occasional squatting, kneeling, or bending.
  • Light to moderate lifting (20-50 lbs)
Perks of working at Summit Clinical Research Solutions:
  • 401k
  • Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
  • 3 weeks of paid time off
  • 14 paid company holidays
  • Scrub voucher (for eligible positions)
  • And more!
Summit Clinical Research Solutions is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.