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Clinical Operations Manager Ophthalmology Jobs (NOW HIRING)

Insperity

Clinical Operations Manager

Phoenix, AZ · On-site

General information Client / Corporate Client Work Mode In-Office Name Clinical Operations Manager Job ID 21898 City Phoenix Published date 02-Jun-2026 State Arizona Country United States Zip Code ...

UC Davis Health

Clinical Operations Manager

Sacramento, CA · On-site

$114K - $236K/yr

The Clinical Operations Manager ensures that all functions operate cohesively in all four pillars: Throughput and Patient Flow, Capacity and Resource Management, Reliability of Care Delivery, Quality ...

Insperity

Clinical Operations Manager

Phoenix, AZ

Description & Requirements Clinical Operations Manager A leading healthcare organization specializing in renal care and outpatient surgical services is seeking an experienced Clinical Operations ...

ADP, Inc.

Clinical Operations Manager

Moreno Valley, CA · On-site

$72K - $85K/yr

Clinical Operations Manager 2 days ago Requisition ID: 1210 Salary Range: $72,000.00 To $85,000.00 Annually Clinical Operations Manager Summary: The Clinical Operations Manager serves as the ...

Newport Academy

Clinical Operations Manager

Monticello, MN · On-site

$92K - $124K/yr

What You'll Do The Clinical Operations Manager works in collaboration with the Operations Manager and other team members to oversee treatment services for their assigned program, ensuring delivery of ...

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Clinical Operations Manager Ophthalmology information

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$35K

$98K

$186.5K

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

As of Sep 13, 2026, the average yearly pay for clinical operations manager ophthalmology 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 cities are hiring for Clinical Operations Manager Ophthalmology jobs?

Cities with the most Clinical Operations Manager Ophthalmology job openings:

What states have the most Clinical Operations Manager Ophthalmology jobs?

States with the most job openings for Clinical Operations Manager Ophthalmology jobs include:

What are popular job titles related to Clinical Operations Manager Ophthalmology jobs?

For Clinical Operations Manager Ophthalmology jobs, the most frequently searched job titles are:

Infographic showing various Clinical Operations Manager Ophthalmology job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $98,039 per year, or $47.1 per hour.

Clinical Operations Manager

Austin, TX • On-site

Pinnacle Clinical Research
Health Care and Social Assistance • 201 - 500 employees
Learn more about Pinnacle Clinical Researchexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Key responsibilities

  • Oversee daily operations of clinical research staff and studies

  • Coordinate multiple projects with competing priorities and deadlines

  • Supervise creation and completion of study-related documents

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!