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Merck Clinical Operations Manager Jobs in Riverside, CA

DaVita, Inc.

Healthcare Operations Manager

Redlands, CA · On-site

$91K - $144K/yr

Develop, mentor and inspire a cross-functional clinical team (census dependent on state laws) to ... Manage complete operation and performance of the clinic: adhere to budget, forecast expenses ...

DaVita

Healthcare Operations Manager

Redlands, CA

$91K - $144K/yr

Develop, mentor and inspire a cross-functional clinical team (census dependent on state laws) to ... Manage complete operation and performance of the clinic: adhere to budget, forecast expenses ...

DaVita

Healthcare Operations Manager

Hesperia, CA · On-site

$96K - $151K/yr

Develop, mentor and inspire a cross-functional clinical team (census dependent on state laws) to ... Manage complete operation and performance of the clinic: adhere to budget, forecast expenses ...

Amae Health

Practice Operations Manager

Orange, CA · On-site

The clinical protocols, the measurement science, the precision medicine, the technology to deliver ... We are hiring a Practice Operations Manager to serve as the operational leader for our two new ...

Amae Health

Practice Operations Manager

Orange, CA · On-site

The clinical protocols, the measurement science, the precision medicine, the technology to deliver ... We are hiring a Practice Operations Manager to serve as the operational leader for our two new ...

PathWell Health

Home Health Clinical Manager

Upland, CA · On-site

A home health clinical manager is responsible for overseeing and managing the clinical operations of a home health agency. This role requires a strong background in healthcare, as well as excellent ...

Pathwell Health

Home Health Clinical Manager

Upland, CA · On-site

$120K/yr

) A home health clinical manager is responsible for overseeing and managing the clinical operations of a home health agency. This role requires a strong background in healthcare, as well as excellent ...

Pathwell Health

Home Health Clinical Manager

Upland, CA · On-site

$90K - $120K/yr

A home health clinical manager is responsible for overseeing and managing the clinical operations of a home health agency. This role requires a strong background in healthcare, as well as excellent ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II ...

AbbVie

Study Project Manager II

Irvine, CA · On-site

$124K/yr

Leading the delivery of clinical operational strategies to ensure studies are executed with quality and efficiency, on-time, within budget, and meet company objectives. The Study Project Manager II ...

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All JobsMerck Clinical Operations JobsMerck Clinical Operations Manager JobsMerck Clinical Operations Manager Jobs in Riverside, CA

Merck Clinical Operations Manager information

See Riverside, CA salary details

$36.5K

$102.3K

$194.6K

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

As of Aug 15, 2026, the average yearly pay for merck clinical operations manager in Riverside, CA is $102,281.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $118,400.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Merck clinical operations manager, and why are they important?

To thrive as a Merck Clinical Operations Manager, you need a strong background in clinical research, project management, and a relevant degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory compliance, and certifications like PMP or GCP are commonly required. Exceptional leadership, problem-solving, and communication skills distinguish top performers in this role. These skills ensure the effective execution of clinical trials, regulatory adherence, and successful cross-functional team collaboration.

What does a Merck clinical operations manager do?

A Merck Clinical Operations Manager oversees the planning, execution, and management of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory requirements. They coordinate cross-functional teams, manage budgets and timelines, and serve as a key liaison between internal stakeholders and external partners. Their role is critical in ensuring that clinical studies generate reliable data to support the development and approval of new medicines.

How does a Merck clinical operations manager typically collaborate with cross-functional teams during a clinical trial?

As a Clinical Operations Manager at Merck, you will regularly collaborate with cross-functional teams such as clinical research associates, data management, regulatory affairs, medical writing, and biostatistics. Your role involves facilitating clear communication to ensure trial milestones are met, addressing operational challenges, and aligning on project goals. You will often lead meetings, coordinate with internal and external stakeholders, and ensure that all teams are updated on timelines, compliance, and protocol changes. This collaborative environment is essential for delivering high-quality clinical studies efficiently and in accordance with regulatory standards.

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

AspectMerck Clinical Operations ManagerMerck Clinical Research Associate
ResponsibilitiesOversees clinical trial operations, manages teams, ensures compliance, and coordinates with stakeholders.Supports site activities, monitors trial progress, and ensures data accuracy at clinical sites.
Required CredentialsBachelor's degree in life sciences, project management experience, knowledge of GCP guidelines.Bachelor's degree in health sciences or related field, clinical trial monitoring experience.
Work EnvironmentOffice-based with site visits, team management, strategic planning.Primarily site visits, monitoring activities, and data collection.

The Merck Clinical Operations Manager focuses on overseeing entire clinical trial processes and managing teams, while the Merck Clinical Research Associate primarily supports site-level activities and monitors trial progress. Both roles require relevant clinical experience and knowledge of GCP guidelines, but differ in scope and responsibilities.

What are popular job titles related to Merck Clinical Operations Manager jobs in Riverside, CA?

For Merck Clinical Operations Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Merck Clinical Operations Manager jobs in Riverside, CA look for?

The top searched job categories for Merck Clinical Operations Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Merck Clinical Operations Manager jobs?

Cities near Riverside, CA with the most Merck Clinical Operations Manager job openings:

Merck Clinical Operations Manager jobs near you

Clinical Study Administrator

Motion Recruitment Partners, LLC

Irvine, CA • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New

Job description

Kelly Science and Clinical FSP is currently seeking a Clinical Study Administrator for a long-term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Job Description
Position Title: Clinical Study Administrator
Division: Clinical Operations
Reports To: Study Team Lead
Job Function Summary Overview:
This individual will provide support to the clinical study staff within Clinical Operations
Perform a variety of clinical research operations duties of a routine and technical nature in support of clinical trials.
Supports project managers within the assigned clinical studies.
Key Job Activities: Under direction of Clinical Operations personnel, and in accordance with all applicable Regional, state and local laws/regulations and corporate procedures and guidelines, this position will
  • As directed, provides support to the project teams which may include tracking study data, following-up with clinical sites on essential documents; assist in drafting and distributing study mailings, including study newsletters; assist in drafting of agenda/meeting minutes and scheduling of meetings.
  • Assist in payments/tracking for patient reimbursements.
  • Performs data entry in systems
  • Run reports including training matrix reports, metrics for management reviews
  • Support management of IRB/IEC renewal compliance.
  • Coordinate process for the review of study data, such as MRIs, by third-party vendors.
  • Assist in ordering, shipping, tracking of, study supplies including, but not limited to, investigational devices and site binders. Maintain master device accountability log as requested.
  • Assist with scheduling and organizing investigators and expert panel meetings.
  • Assist with file reviews and Audit preparation
  • Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
  • Work with management group to help achieve department goals.
  • Participate in process improvement activities within the department.
  • May be involved in other tasks to support Clinical Operations and Operating Company as needed.

Other Administrative Tasks
  • Know, understand, incorporate, and comply with all applicable laws and regulations relating to business activities and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
  • May be asked to provide additional support to Clinical Operations staff, as needed.
Job Qualifications
Education
  • Minimum of a Bachelor's Degree is required.

Experience
  • Previous clinical research experience
  • Requires previous administrative support experience or equivalent for at least 1 year.
  • Clinical/medical background

Knowledge
  • Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point).
Additional Requirements
  • Demonstrated competencies in the following areas are required:
    • Tracking
    • Written and verbal communications
    • Attention to details
    • Organizational skills

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