Top 27 Clinical research manager Jobs in Paradise Valley, Az

Clinical Research, Clinical Safety Manager
Castle Biosciences —Phoenix, AZ
- Online Application
- Nursing
- Office
- Bachelor's degree
- Health savings account
- Paid holidays
Quick Apply
Manager - Clinical Trials
HonorHealth —Scottsdale, AZ
- Full-time
- Master's degree
- Bachelor's degree
- Recruiting
Associate Manager / Manager / Senior Manager, Clinical Operations
Imaging Endpoints —Scottsdale, AZ
- Writing skills
- Bachelor's degree
- Organizational skills
Clinical Data Manager
Imaging Endpoints —Scottsdale, AZ
- Analysis skills
- Bachelor's degree
- Continuous improvement
Senior Global Clinical Study Manager
IQVIA —Phoenix, AZ
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Research Project Manager
St Joseph Hospital & Medical Center —Phoenix, AZ
- $32.38 - $48.17 an hour
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Research Program Manager - Investigator Initiated Studies
HonorHealth —Scottsdale, AZ
- Full-time
- Office
- 3 years
- Master's degree
Lead Clinical Research Coordinator
ECN Operating LLC —Sun City, AZ
- Weekends as needed
- Mid-level
- Organizational skills
- Leadership
Quick Apply
3d
Manager, Clinical & Business Insight (Data Analytics)
TriWest Healthcare Alliance —Phoenix, AZ
- $124,000 - $134,000 a year
- Full-time
- Microsoft Access
- Microsoft Outlook
- Computer literacy
- AD&D insurance
- Disability insurance
8d
Imaging Project Manager
Imaging Endpoints —Scottsdale, AZ
- Writing skills
- Mid-level
- Bachelor's degree
Study Manager I
DM CLINICAL RESEARCH GROUP —Phoenix, AZ
- Customer service
- 5 years
- Writing skills
7d
Clinical Domain Project Manager (PBM)
Briljent —Phoenix, AZ
- Urgently hiring
- Remote
- Background check
- 7 years
- Continuous improvement
- AD&D insurance
- Disability insurance
Quick Apply
8d
Manager/Senior Manager, Change and Project Management
Imaging Endpoints —Scottsdale, AZ
- Bachelor's degree
- Travel
- Mentoring
Manager – Imaging Clinical Trial Management Systems
Imaging Endpoints —Scottsdale, AZ
- Computer literacy
- Writing skills
- SQL
Project Lead - RUA92307
IQVIA —Phoenix, AZ
- $200,000 - $225,000 a year
- Full-time
- Nursing
- Driver's License
- Travel
12d
Senior Imaging Project Manager
Imaging Endpoints —Scottsdale, AZ
- Writing skills
- Bachelor's degree
- Mentoring
Manager Sponsor Regulatory Affairs & Institutional Trial Compliance
HonorHealth —Scottsdale, AZ
- Full-time
- Office
- 3 years
- Master's degree
Site Network Manager (North America)
Alimentiv —Phoenix, AZ
- $97,500 - $163,000 a year
- Full-time
- Remote
- Nursing
- 7 years
- Bachelor's degree
Quick Apply
Mental Health Clinical Supervisor
Thrivewell Health Centers —Glendale, AZ
- $78,000 - $82,000 a year
- Full-time
- Experience working with individuals with developmental disabilities
- HIPAA
- Experience working with children
- Health insurance
Quick Apply
CRC Operations Lead
The Specialty Alliance —Litchfield Park, AZ
- Full-time
- Writing skills
- Office
- Business development
Quick Apply

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Clinical Research, Clinical Safety Manager

Castle Biosciences -
Phoenix, AZ

Quick Apply

Job Details

Full-time

Benefits

Health savings account
Paid holidays
Health insurance
Paid time off
401(k) 6% Match
401(k) matching

Qualifications

Healthcare incident report preparation
Adverse event reporting
Clinical trial risk management
Safety regulations
Clinical research protocol review
Bachelor's degree
Adverse drug reaction monitoring
Biomedical regulatory compliance
Communication with regulatory authorities for clinical trials
Clinical quality assurance standards
FDA regulations
Laboratory compliance and regulatory documentation

Full Job Description

Castle Biosciences Earns "Top Workplaces USA Award" for Phoenix, Pittsburgh, and Friendswood!

Learn more at www.CastleBiosciences.com

Castle Biosciences Inc. is growing, and we are looking to hire a full-time Clinical Research, Clinical Safety Manager working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office location, with a start date of August 1, 2026.

Why Castle Biosciences?

Exceptional Benefits Package:

Excellent Annual Salary + 20% Bonus Potential
20 Accrued PTO Days Annually + 10 Paid Holidays
401K with 100% Company Match up to 6%
3 Health Care Plan Options + Company HSA Contribution
Company Stock Grant Upon Hire

A DAY IN THE LIFE OF AN Clinical Safety Manager

The Clinical Research Safety Manager is responsible for establishing, implementing, and continuously improving clinical research safety processes for a laboratory-developed test (LDT) and medical device organization while ensuring compliance with applicable regulations, Company policies, and Standard Operating Procedures (SOPs). This role serves as the operational safety lead for company-sponsored clinical studies, overseeing safety planning, adverse event management, risk assessments, safety reporting, and regulatory documentation for FDA-regulated LDT, IVD, and medical device studies. The position partners with cross-functional teams to ensure participant safety, regulatory compliance, inspection readiness, and alignment between clinical safety activities, quality systems, and post-market processes. This individual contributor role also supports the development of safety processes, study documentation, and training while providing support as directed by leadership and contributing to the growth of the clinical research safety function.

REQUIRED QUALIFICATIONS

Bachelor's degree in life sciences, nursing, clinical research, biomedical sciences, regulatory/quality, public health, or related field.
5+ years of clinical research, clinical safety, medical device/IVD, diagnostics, regulatory, quality, or related experience in a regulated healthcare environment.
Demonstrated experience supporting sponsor-led clinical studies, preferably device/IVD/LDT studies, including protocol review, safety reporting pathways, IRB/EC interactions, and study documentation.
Working knowledge of FDA clinical research and medical device requirements, including 21 CFR Parts 803, 812, and 820 and applicable safety/reporting expectations.
Experience evaluating and documenting adverse events, serious adverse events, unanticipated problems, unanticipated adverse device effects, protocol-defined events, deviations, and safety issues.
Please see the full job description at the end of the job ad.

SCHEDULE

Monday-Friday, 40 hours per week, working from our Phoenix, AZ, Friendswood, TX or Pittsburgh, PA office locations.
Occasional overnight travel, up to 10%, may be required to support site engagement, audits/inspections, study meetings, training, or conferences.

READY TO JOIN OUR BIOTECH TEAM?

We truly appreciate your time. If this feels like the right opportunity for you, we'd love for you to complete our mobile-friendly application. We're excited to learn more about you and look forward to connecting soon!

Castle Biosciences Awards and Research Developments!

WORK AUTHORIZATION

All candidates must be legally authorized to work in the United States. Currently, Castle Biosciences does not sponsor H-1B visas, OPT, or employment-related visas.

ABOUT CASTLE BIOSCIENCES INC.

At Castle, it all comes down to people. After all, disease doesn't just happen - it happens to people. We believe that disease management and treatment decisions can be better informed through a person's unique biology, which is revealed through the scientific rigor of our innovative, laboratory-developed tests. We are committed to empowering healthcare providers and patients with the goal of improved outcomes.

Every employee at Castle has an impact on patient care, and we work to ensure that everyone finds their work to be both challenging and rewarding. We behave with integrity and treat our colleagues with respect and kindness. Our culture fosters an environment of trust, transparency, and collaboration. We prioritize and encourage internal growth and professional development.

Castle Biosciences is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.

If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail [email protected].

This email was created exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only messages left for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.

** No third-party recruiters, please

Quick Apply

Refine Your Search

clinical research manager jobs in paradise valley, az

Clinical Research, Clinical Safety Manager

Manager - Clinical Trials

Associate Manager / Manager / Senior Manager, Clinical Operations

Clinical Data Manager

Senior Global Clinical Study Manager

Research Project Manager

Research Program Manager - Investigator Initiated Studies

Lead Clinical Research Coordinator

Manager, Clinical & Business Insight (Data Analytics)

Imaging Project Manager

Study Manager I

Clinical Domain Project Manager (PBM)

Manager/Senior Manager, Change and Project Management

Manager – Imaging Clinical Trial Management Systems

Project Lead - RUA92307

Senior Imaging Project Manager

Manager Sponsor Regulatory Affairs & Institutional Trial Compliance

Site Network Manager (North America)

Mental Health Clinical Supervisor

CRC Operations Lead

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