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Clinical Project Manager Jobs in Riverside, CA (NOW HIRING)

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of ... Work closely with clinical project team and database programmers to provide edit check requirements ...

Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management. * Apply experience to analyze clinical study data, including statistical ...

Plans, tracks and manages assigned monitoring project budgets to ensure adherence to business plans * Ensures resources assigned to designated clinical trials to provide quality deliverables while ...

Plans, tracks and manages assigned monitoring project budgets to ensure adherence to business plans * Ensures resources assigned to designated clinical trials to provide quality deliverables while ...

Projects include formal large quoting projects or those involving custom products. Serve as a ... Work with external teams of Sales Reps, Sr. Sales Specialists, Sales Management, Clinical team, IDN ...

Projects include formal large quoting projects or those involving custom products. Serve as a ... Work with external teams of Sales Reps, Sr. Sales Specialists, Sales Management, Clinical team, IDN ...

Projects include formal large quoting projects or those involving custom products. Serve as a ... Work with external teams of Sales Reps, Sr. Sales Specialists, Sales Management, Clinical team, IDN ...

Job Title: Project Manager Job Location: Pomona, CA 91768 Job Duration: 18 Months Shift/Schedule: Hybrid 2 days in the office Job Responsibilities: * Project Management oversight and function ...

Application Development Project Management Quality Assurance Business/Systems Analysis Datawarehouse & Business Intelligence Infrastructure & Network Services Risk Management & Compliance Business ...

... scale-up, clinical testing, and ultimately U.S. market launch. The ideal candidate brings deep ... Technical Project Management Oversee day-to-day execution of technical workstreams including ...

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Clinical Project Manager information

See Riverside, CA salary details

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$63

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How much do clinical project manager jobs pay per hour?

As of May 29, 2026, the average hourly pay for clinical project manager in Riverside, CA is $63.33, according to ZipRecruiter salary data. Most workers in this role earn between $44.13 and $74.23 per hour, depending on experience, location, and employer.

What Does a Clinical Project Manager Do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What are the key skills and qualifications needed to thrive as a Clinical Project Manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What are some common challenges Clinical Project Managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What are the most commonly searched types of Clinical Project jobs in Riverside, CA? The most popular types of Clinical Project jobs in Riverside, CA are:
What are popular job titles related to Clinical Project Manager jobs in Riverside, CA? For Clinical Project Manager jobs in Riverside, CA, the most frequently searched job titles are:
What cities near Riverside, CA are hiring for Clinical Project Manager jobs? Cities near Riverside, CA with the most Clinical Project Manager job openings:
Sr. Analyst Clinical Project Management

Sr. Analyst Clinical Project Management

Edwards Lifesciences Corporation

Irvine, CA

$92K - $130K/yr

Full-time

Posted 10 days ago


Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

62nd of 511 rated manufacturers


Job description

The Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is dedicated to solving the complex challenges of mitral and tricuspid disease, to transform treatment and to significantly improve patients' lives. This is an exciting opportunity for an experienced and exceptional project management professional to join a team that is boldly designing transcatheter mitral and tricuspid therapies from the ground up. The Project Management Office (PMO) in the Transcatheter Mitral Valve Replacement (TMVR) therapy team has the responsibility to lead strategic programs that support the development, growth and adoption of our growing mitral replacement franchise.

The Sr. Analyst, Clinical Project Management will lead strategic planning, governance, and operational excellence across the TMTT evidence functions. This role ensures that clinical evidence programs are delivered with rigor, transparency, and alignment to TMVR and TMTT's longterm portfolio strategy.

How you'll make an impact:

You will partner closely with Clinical Affairs, Medical Affairs, R&D, Regulatory, and Marketing to ensure evidence generation is coordinated, prioritized, and executed with discipline. This is a highvisibility leadership role for someone who thrives in a fastmoving, sciencedriven environment.
Responsible for program scope, performance, dependency management, proactive risk and issue management and resolution, as well as clear communication to stakeholders.

Establish and manage effective working relationships with other project managers assigned to numerous simultaneous departmental projects to ensure continued program health.

Lead and coordinate multiple parallel workstreams (as defined in the project management plan) across departments and functions involved in evidence initiatives.

Lead the execution of tasks and actively manage project risk.

Assess project performance to monitor the program progress, identify and quantify variances, perform required corrective actions and communicate to all stakeholders.

Establish and coordinate team members and stakeholder relationships, expectations, and communications.

Manage project closure activities, including gathering and disseminating lessons learned.

Support additional TMVR PMO process improvement activities as needed.

Other duties as assigned by Leadership

What you'll need (Required):
Bachelor's Degree in related field, 5 Years hands on experience managing mid-to-large scale projects or equivalent work experience.
Project Management Professional (PMP) is Preferred

What else we look for (Preferred):

Medical Device or Clinical Study Management experience is a must.

Clinical Trial Management is preferred.

Proven expertise in usage of MS Office Suite and related project management systems
Excellent documentation and communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
Substantial understanding and knowledge of principles, theories, and concepts relevant to managing small-to-mid scale project plans
Ability to adapt to new technologies
Ability to adapt to rapidly changing environment
Strong problem-solving, organizational, analytical and critical thinking skills
Ability to work in a fast paced environment and multi-task
Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations
Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $92,000 to $130,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.


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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958