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Clinical Science Manager Jobs in Arizona (NOW HIRING)

Caris MPI, Inc.

Clinical Data Product Owner

Phoenix, AZ · On-site

$120 - $180/hr

Backed by cutting-edge molecular science and AI, we ask ourselves every day: "What would I do if ... Lead the design and development of new product features, and manage data-privacy certification ...

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University of Florida

The UF Health network of hospitals and physician practices manages more than 3 million inpatient ... The college's 16 clinical science departments house more than 500 faculty members, 1,560 staff and ...

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Clinical Science Manager information

See Arizona salary details

$40.5K

$76.7K

$130.5K

How much do clinical science manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical science manager in Arizona is $76,741.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,600.00 and $83,400.00 per year, depending on experience, location, and employer.

What is a clinical science manager?

Clinical Science Managers are professionals who oversee and coordinate clinical research projects, often within the pharmaceutical, biotechnology, or medical device industries. They are responsible for managing clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams such as clinical operations, regulatory affairs, and medical affairs. Their role involves protocol development, data analysis, and ensuring the safety and efficacy of investigational products. Clinical Science Managers also play a critical part in interpreting study results and presenting findings to stakeholders. They typically have advanced degrees in life sciences and significant experience in clinical research.

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

To thrive as a Clinical Science Manager, you need a solid background in clinical research, life sciences, and project management, typically supported by an advanced degree (e.g., PharmD, PhD, or MD) and industry experience. Familiarity with clinical trial management systems, regulatory compliance tools, and data analysis platforms is crucial. Strong leadership, strategic thinking, and effective communication skills help you manage cross-functional teams and build relationships with stakeholders. These competencies ensure the successful design, execution, and oversight of clinical studies, ultimately advancing scientific and business goals.

How does a clinical science manager typically collaborate with cross-functional teams during clinical trial development?

Clinical Science Managers play a key role in bridging scientific objectives with operational execution by working closely with clinical operations, regulatory affairs, data management, and medical affairs teams. They often lead the development of clinical protocols and ensure scientific integrity throughout the study, facilitating regular meetings and communication to align project goals and timelines. Their collaborative efforts help anticipate and resolve challenges, streamline processes, and ensure that trials meet regulatory requirements and scientific standards.

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

AspectClinical Science ManagerClinical Research Associate
CredentialsTypically requires advanced degrees (e.g., Master’s or PhD) and industry experienceUsually holds a bachelor’s degree in life sciences or related field
Work EnvironmentLeads teams, manages projects, and oversees clinical studiesMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical, biotech, and medical device companiesContract research organizations, pharmaceutical companies
Search & Comparison IntentUnderstanding managerial roles in clinical scienceFocus on trial monitoring and site management

The Clinical Science Manager typically oversees clinical projects and manages teams, requiring advanced credentials. In contrast, the Clinical Research Associate focuses on monitoring clinical trials at sites. Both roles are essential in the clinical research process but differ in responsibilities and experience levels.

What are popular job titles related to Clinical Science Manager jobs in Arizona?

For Clinical Science Manager jobs in Arizona, the most frequently searched job titles are:

What job categories do people searching Clinical Science Manager jobs in Arizona look for?

The top searched job categories for Clinical Science Manager jobs in Arizona are:

What cities in Arizona are hiring for Clinical Science Manager jobs?

Cities in Arizona with the most Clinical Science Manager job openings:

Clinical Science Manager jobs near you
Infographic showing various Clinical Science Manager job openings in Arizona as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $76,741 per year, or $36.9 per hour.

Clinical Science Program Specialist

IT Engagements

Tucson, AZ • On-site

Contractor

Re-posted 12 days ago

Job description

Greetings from IT Engagements
 
 IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.
 
Job Summary
 
Job Title: Clinical Science Program Specialist
Work Location: 1910 East Innovation Park Drive, Tucson, AZ USA - 85755
 
The Opportunity
  • Manages multiple clinical testing and lab services projects from initiation through contract completion under
    supervision of Program Manager. Acts as primary point of contact to Pharma customers.
  • Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and:
    - Develops project plans, establish and coordinates timelines for assigned projects and functions;
    - Manages execution of cross-functional plans and tracks progress of activities;
    - Identifies gaps, potential bottlenecks or delays and challenge assumptions.
  • Oversees and guides day to day activities of sample process flow and accurate reporting of results.
    Implements / pulls in best practices within the clinical sciences team; fosters continuous improvement by
    ensuring knowledge and experience exchange
  • Guides and manages cross-functional interactions to complete the assigned projects within the deadline.
  • Interfaces with resources outside of the company (Contract Research Organizations (CROs), site
    investigators, client counterparts, etc.) and serves as single point of contact with Pharma and Roche clients.
  • Manages meeting activities such as setting agendas, organizing meeting time and editing meeting minutes.
  • Tracks, maintains and communicates project reports and clinical study data to Pharma and Roche clients.
Requirements
  • At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation
  • Exposure to clinical studies
  • Experience with clinical projects that require rapid activity/milestone achievement.
  • Strong communication, collaboration, and organizational skills are required
  • Bachelor's degree is required (Life Sciences is preferred)
Preferred
  • Previous experience with standard project management process (PMI) desired.
  • Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred.
  • Preferred experience in clinical studies or companion diagnostics
  • Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.
Regards,
Satya
Satya@Itengagements.com