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Clinical Program Manager Jobs in Sandy, UT (NOW HIRING)

Amgen

Imaging Specialist Manager

Salt Lake City, UT · On-site +1

IMAGING SPECIALIST MANAGER LIVE What you will do In this vital role you will plan and execute ... Serve as an internal subject matter expert, advising Clinical Program Operations (CPO), and other ...

Imh

Linen Field Logistics Specialist

Lehi, UT · On-site

$18.76 - $24.38/hr

This position is responsible for overseeing inventory management activities for assigned departments or clinical programs. Key duties include distributing and managing supplies to ensure that medical ...

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All JobsClinical Program JobsClinical Program Manager JobsClinical Program Manager Jobs in Sandy, UT

Clinical Program Manager information

See Sandy, UT salary details

$42.3K

$88K

$142.1K

How much do clinical program manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical program manager in Sandy, UT is $87,997.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,900.00 and $99,800.00 per year, depending on experience, location, and employer.

What is a clinical program manager?

A Clinical Program Manager is a professional responsible for overseeing the planning, coordination, and execution of clinical trials or healthcare programs within a medical or research organization. They ensure that clinical projects meet regulatory, ethical, and organizational standards, while managing timelines, budgets, and cross-functional teams. Clinical Program Managers also liaise with stakeholders, analyze data, and report on project progress to ensure successful outcomes. Their role is critical in advancing medical research and improving patient care.

What are the key skills and qualifications needed to thrive as a clinical program manager?

To thrive as a Clinical Program Manager, you need a solid background in clinical research or healthcare management, often supported by a relevant degree and experience in program coordination. Familiarity with clinical trial management systems (CTMS), regulatory compliance protocols, and sometimes certifications like PMP or CCRA are commonly required. Strong leadership, organizational skills, and effective communication set top performers apart in this role. These skills are crucial for overseeing complex clinical programs, ensuring regulatory adherence, and leading multidisciplinary teams toward successful project outcomes.

How does a clinical program manager typically collaborate with cross-functional teams to ensure successful clinical trial execution?

A Clinical Program Manager works closely with cross-functional teams, including clinical research associates, data managers, regulatory affairs, and medical monitors, to coordinate all aspects of clinical trials. They facilitate regular meetings, ensure clear communication, and resolve any issues that may affect timelines or data quality. This role is pivotal in aligning diverse team members toward shared goals, managing expectations, and adapting to evolving study requirements, which helps drive successful trial outcomes.

What is the difference between Clinical Program Manager vs Clinical Project Manager?

AspectClinical Program ManagerClinical Project Manager
CredentialsTypically requires a clinical background, such as RN, MSN, or related healthcare degree, along with project management certificationOften requires a project management certification (PMP) or equivalent; clinical background is preferred but not always mandatory
Work EnvironmentOversees multiple related projects within a clinical program, often in healthcare organizations or pharmaceutical companiesManages individual clinical trials or projects, usually within a larger program or portfolio
Employer & Industry UsageCommonly employed in healthcare, biotech, and pharmaceutical industries to coordinate broad clinical initiativesUsed across similar industries to manage specific clinical studies or trials

The Clinical Program Manager focuses on overseeing multiple related clinical projects and strategic initiatives, while the Clinical Project Manager manages individual clinical trials. Both roles require project management skills, but the Program Manager has a broader scope and strategic responsibilities.

How much do clinical program managers make?

Clinical Program Managers in California typically earn between $100,000 and $150,000 annually, depending on experience, certifications, and the size of the organization. Salaries can vary based on the complexity of clinical programs and the level of responsibility involved.

What degree do I need to be a clinical program manager?

A clinical program manager typically needs at least a bachelor's degree in a healthcare-related field such as nursing, public health, or healthcare administration. Many employers prefer candidates with a master's degree, such as an MBA or a master's in healthcare administration, along with relevant experience and strong project management skills. Certifications like PMP or RAC may also enhance qualifications for this role.

What does a clinical program manager do?

A clinical program manager oversees the planning, implementation, and management of clinical trials and research programs. They coordinate teams, ensure compliance with regulatory standards, and monitor project progress using tools like project management software. Strong organizational, communication, and regulatory knowledge are essential for success in this role.

What are the most commonly searched types of Clinical Program jobs in Sandy, UT?

The most popular types of Clinical Program jobs in Sandy, UT are:

What cities near Sandy, UT are hiring for Clinical Program Manager jobs?

Cities near Sandy, UT with the most Clinical Program Manager job openings:

Clinical Program Manager jobs near you
Infographic showing various Clinical Program Manager job openings in Sandy, UT as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 18% Part Time, and 3% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $87,997 per year, or $42.3 per hour.

Imaging Specialist Manager

Amgen

Salt Lake City, UT • On-site, Remote

Full-time

Posted 12 days ago

Key responsibilities

  • Plan and execute imaging operations for clinical trials globally.

  • Manage and coordinate the operational imaging strategy, including planning, risk assessment, mitigation, and execution for clinical trials.

  • Provide oversight and expertise for imaging setup, startup activities, and maintain the quality and scientific integrity of imaging-related elements in clinical trials.

Job description

Career CategoryClinicalJob Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel likeyou'repart of something bigger,it'sbecause you are. AtAmgenour shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together-researching,manufacturingand delivering ever-better products that reachover10 million patientsworldwide.It'stime for a career you can be proud of. Join us.

IMAGING SPECIALIST MANAGER

LIVE

What you will do

In this vital role you will plan and execute imaging operations for clinical trials globally. You will manage and coordinate the operational imaging strategy, plan, risk assessment, mitigation, and execution for oncology and non-oncology clinical trials across all phases from study start-up to close-out.

Responsabilities:

  • Provide oversight and expertise for imaging setup and startup activities

  • Maintain the quality and scientific integrity of imaging-related elements in clinical trials

  • Working with the Imaging Scientist Team within Clinical Biomarkers & Diagnostics to enable E2E Imaging specialist support throughout the portfolio

  • Serve as an internal subject matter expert, advising Clinical Program Operations (CPO), and other Global Development Operations (GDO) functions, on best practices, ensuring consistent standards and key lessons learned are applied across the portfolio for continuous improvement and maximum impact of the solutions

  • Build global cross-functional relationships and collaborate with clinical teams to integrate imaging into trials and update senior management

WIN

What we expectofyou

We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:

  • Experience in life sciences or medical fields, including imaging expertise and clinical research acquired working on clinical trials at a biotech, pharmaceutical or CRO company, having a strong understanding of clinical development programs in a global setting

  • Experience at or oversight of outside clinical research vendors (CRO's, central labs, imaging vendors, etc.)

  • Experience in operationalizing global clinical studies with imaging and vendor management

  • Good understanding of quality oversight and process improvement

  • Ability to network and establish relationships cross-functionally

  • Project and Program management and phenomenal communication skills

  • Degree educated

THRIVE

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates' professional and personal growth and well-being.

  • Vast opportunities to learn and move up and across our global organization

  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Location: Ability to work remotely from UK/US.

APPLY NOW

for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

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