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Merck Clinical Operations Manager Jobs in Azusa, CA

SoCal Eye

Clinic Operations Manager

Long Beach, CA · On-site

$85 - $100/hr

The Clinical Operations Manager owns and drives the daily clinical operations of a well-establish ophthalmology practice, supporting the clinical staff, including ophthalmic assistants, clinical ...

Orion Group

Clinical Operations Support

Orange, CA · On-site

$19 - $23.50/hr

Clinical Operations Support II - Skincare Location: Irvine, CA - 100% Onsite Contract Duration: 12 ... management, and data entry . The ideal candidate will have excellent customer service skills ...

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

Merck Clinical Operations Manager information

See Azusa, CA salary details

$35.6K

$99.7K

$189.7K

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

As of Sep 6, 2026, the average yearly pay for merck clinical operations manager in Azusa, CA is $99,739.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,800.00 and $115,500.00 per year, depending on experience, location, and employer.

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

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

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

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

Merck Clinical Operations Manager jobs near you

Clinical Operations Manager

BiVACOR Inc

Huntington Beach, CA • On-site

$118K - $154K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago

Key responsibilities

  • Oversee day-to-day operational logistics for clinical study activities at participating sites

  • Maintain site qualification documentation, essential regulatory binders, and operational SOPs

  • Track site-level operational milestones and flag deviations

Job description

Help Us Build the Future of the Human Heart.

At BiVACOR, we’re developing the world’s most advanced total artificial heart, a technology capable of saving millions of lives around the world. We’re a team united by purpose, working on something truly unprecedented. Every site you prepare, every milestone you track, and every compliance requirement you uphold plays a direct role in giving patients another shot at life. If that’s the kind of work that gets you out of bed in the morning, we think you belong here.

About the Role

This is a high-impact, cross-functional role at the heart of BiVACOR’s clinical program, where your operational expertise will directly shape the success of our first-in-human and pivotal clinical studies. As Clinical Operations Manager, you will be the organizational backbone of site-level activity, ensuring every participating center is prepared, compliant, and ready to support patients receiving the world’s first Total Artificial Heart. You will bring meticulous attention to detail, a deep understanding of clinical trial operations, and a collaborative approach that keeps complex, multi-site programs on track.
Key Responsibilities

  • Oversee day-to-day operational logistics for clinical study activities at participating sites

  • Maintain site qualification documentation, essential regulatory binders, and operational SOPs

  • Track site-level operational milestones and flag deviations

  • Coordinate supply chain activities related to clinical device inventory and investigational materials

  • Support site initiation visits and ensure operational readiness prior to patient enrolment

  • Liaise with clinical research and regulatory affairs on site-level compliance requirements

What You Bring

  • Bachelor’s degree in Life Sciences, Health Sciences, or a related field; advanced degree or CRA/CRC certification preferred

  • 3–5+ years of clinical operations, clinical trial management, or site management experience in a medical device or pharmaceutical environment

  • Solid understanding of ICH-GCP, FDA IDE regulations, and essential document requirements for investigational device studies

  • Experience managing regulatory binders, site qualification documentation, and investigational supply logistics

  • Proficiency with clinical trial management systems (CTMS) and electronic trial master file (eTMF) platforms

  • Can-do attitude — highly organized — strong cross-functional communication and stakeholder management skills

  • Willingness to travel to clinical sites as required; flexibility to support BiVACOR as our program scales

What We Offer

BiVACOR offers a competitive compensation package and comprehensive benefits, including:

  • 401(k) with company matching

  • Medical, dental, and vision insurance

  • Health Savings Account (HSA) & Flexible Spending Account (FSA)

  • Life insurance & Employee Assistance Program

  • Generous paid time off

This role may be based at BiVACOR’s Huntington Beach headquarters. The expected salary range for this position based in Huntington Beach California is $118,000 to $154,000. Actual compensation will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Relocation benefits are not available for this posting.
Apply today and be part of something extraordinary.
BiVACOR is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Compensation Range: $118K - $154K