Top 31 Clinical data manager Jobs in Sacramento Ca

Clinical Data Manager
Agilent Technologies Inc —Sacramento, CA
- $105,280 - $197,400 a year
- Full-time
- Computer Science
- 5 years
- System design
- Work from home
9h
Manager, Business Intelligence & Data Analytics
Sutter Health —Sacramento, CA
- $156,332.80 - $234,478.40 a year
- Weekends as needed
- Computer Science
- 5 years
- Writing skills
Clinical Supervisor (Licensed)
Sacramento Children's Home —Sacramento, CA
- $92,000 a year
- Weekends as needed
- Microsoft Word
- LMFT
- Pass drug screening
- Paid holidays
- Disability insurance
Clinical Research Program Manager
Shriners Hospitals for Children —Sacramento, CA
- $80,246.40 - $155,487.07 a year
- Full-time
- 18 years or older
- Management
- Hospital
Quick Apply
12d
Clinical Research Coordinator II
Shriners Hospitals for Children —Sacramento, CA
- $31.90 - $61.79 an hour
- 18 years or older
- Hospital
- Mid-level
Quick Apply
Site Activation Manager
IQVIA —Rosemont, CA
- $86,500 - $216,000 a year
- Full-time
- Remote
- Bachelor's degree
- Team management
- Mentoring
- Work from home
8h
Senior Project Manager, Data Science Initiatives
The Jackson Laboratory —Sacramento, CA
- $74,772 - $125,184 a year
- Master's degree
- Bachelor's degree
- Mentoring
Quick Apply
Program Director
Westcare —North Highlands, CA
- $80,000 - $86,000 a year
- Full-time
- CPR Certification
- Current TB test
- Addiction Medicine
Quick Apply
Applied AI Health Data Architect-Senior Manager
PRICE WATERHOUSE COOPERS —Sacramento, CA
- $124,000 - $280,000 a year
- HIPAA
- 8 years
- SQL
- Paid holidays
- Health insurance
Mental Health Wraparound Program Supervisor - THRIVE FSP
Bay Area Community Services —Sacramento, CA
- $90,000 a year
- Day shift
- Clean driving record
- Customer service
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Sacramento, CA
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification
Applied AI Health Data System Engineer-Senior Manager
PRICE WATERHOUSE COOPERS —Sacramento, CA
- $124,000 - $280,000 a year
- 6 years
- HIPAA
- SQL
- Paid holidays
- Health insurance
Applied AI Health System Engineer – Senior Manager
PRICE WATERHOUSE COOPERS —Sacramento, CA
- $124,000 - $280,000 a year
- Azure
- HIPAA
- 8 years
- Paid holidays
- Health insurance
Licensed Clinical Social Worker
UC Davis Health —Sacramento, CA
- $53.85 - $71.07 an hour
- Overtime
- Acute care
- Background check
- Master of Social Work
- Continuing education credits
- Paid holidays
12d
ConvergeHEALTH - Commercial Life Sciences, Delivery Manager - Managed Platform as a Services (MPaaS) - Innovation_Delivery_Transformation
Deloitte —Sacramento, CA
- $134,500 - $265,100 a year
- Full-time
- Maintenance
- 3 years
- Bachelor's degree
Clinical Team Lead Supervisor
EL HOGAR COMMUNITY SERVICES INC —Sacramento, CA
- $45.00 - $47.25 an hour
- Full-time
- LMFT
- Spanish
- Licensed Clinical Social Worker
Program Manager II/III, FIT Citrus Heights
Stanford Sierra Youth & Families —Citrus Heights, CA
- $85,000 - $115,000 a year
- On call
- LMFT
- Doctoral degree
- Computer literacy
- Flexible schedule
Quick Apply
Program Director *Licensed* - Hope Cooperative (TLCS, Inc.)
Hope Cooperative (aka TLCS, Inc.) —Sacramento, CA
- $4,384.94 - $5,329.92 a month
- Weekends as needed
- Addiction Medicine
- Adults
- HIPAA
- Continuing education credits
- Health savings account
Quick Apply
Clinical Manager
Hope Cooperative (TLCS, Inc.) —Sacramento, CA
- $41.72 - $43.80 an hour
- Overtime
- LMFT
- Addiction Medicine
- Licensed Clinical Social Worker
- Continuing education credits
- Health savings account
Quick Apply
Clinical Team Supervisor
Pacific Clinics —Sacramento, CA
- $87,423 - $107,519 a year
- Weekends as needed
- Bilingual
- LMFT
- Addiction Medicine
- Health insurance
- Dental insurance

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Clinical Data Manager

Agilent Technologies Inc -
Sacramento, CA

Apply Now

Job Details

Full-time
$105,280 - $197,400 a year
9 hours ago

Benefits

Work from home

Qualifications

Biomedical regulatory compliance

Full Job Description

Job Description

We are searching for an experienced Clinical Data Manager to work within the in-vitro diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.

The Clinical Data Manager will plan and oversee all data management activities across assigned studies related companion diagnostics (CDx) development to ensure timely, accurate, and compliant data delivery. They will develop data transfer specifications, support the development of data transfer agreements, manage CRF/EDC systems, perform instream data monitoring, and maintain data in reporting platforms. The role will collaborate with cross-functional teams and external partners to resolve queries and uphold relevant quality standards and regulatory requirements. Additionally, they will author data management documentation, monitor data integrity, implement process improvements, and work on multiple complex projects to support successful CDx activities.

Responsibilities include but are not limited to:

Lead end-to-end clinical data management activities for companion diagnostic studies, including data acquisition, database design, data review, external data integration, reconciliation, quality control, database lock, and preparation of submission-ready datasets supporting global regulatory submissions.

Lead EDC/CRF system design, validation, user acceptance testing (UAT), maintenance, and database lock activities to support CDx study regulatory reporting requirements in accordance with applicable regulatory requirements and company procedures.

Collaborate with Biostatistics and Programming functions to ensure development of submission-ready SDTM and ADaM datasets supporting PMA, 510(k), De Novo, NDA and BLA submissions.

Support preparation of submission-ready clinical data packages for FDA PMA, PMA supplement, 510(k), NDA/BLA companion diagnostic submissions, and international regulatory filings including EU IVDR.

Apply risk-based data management principles to identify critical data and proactively mitigate data quality risks throughout study execution.

Ensure inspection readiness through maintenance of complete, traceable, and auditable records, and serve as a clinical data management SME during audits and regulatory inspections.

Develop Data Transfer Specifications detailing deliverables, formats, and timelines; act as the primary liaison for internal teams and pharmaceutical partners.

Author and maintain data management documentation throughout the study lifecycle, including SOPs, process flows, data management plans, CRFs, and database specifications.

Serve as a subject matter expert (SME) representing Agilent externally and OCMO internally, collaborating with cross-functional teams (Clinical Development, Clinical Operations, CROs, Pharmaceutical Partners, Biostatistics, Quality Affairs/Design Assurance, and Regulatory Affairs) to align on data-related activities and ensure accurate, compliant, and timely data transfers.

Demonstrate expertise in data format standards (e.g., CDISC SDTM ADaM and LAB) and integration with various EDC platforms.

Perform quality control checks to ensure accurate, complete, and compliant data for Agilent internal projects and external data deliverables to pharmaceutical partners.

Identify and escalate data integrity issues; recommend process improvements as needed.

Plan, coordinate, and manage data management activities across programs to maintain consistency in clinical data standards.

Act as Data Management Subject Matter Expert for Agilent’s BioPharma CDx Services Lab (BCSL)

Apply strong knowledge of GCP, ICH, and regulatory requirements to support CDx submissions and communicate effectively to build internal programs.

Qualifications

Bachelor's Degree in Data Science, Computer Science, Information Technology or related field OR Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields with data management experience. Advanced degree preferred.

Minimum 5-8 years of clinical data management experience in biotechnology, pharmaceutical, medical device, diagnostics, or companion diagnostic development.

Hands-on experience with CDISC standards including SDTM, ADaM, CDASH and Define.xml.

Demonstrated experience designing and managing studies using EDC platforms such as Medidata Rave, Veeva CDMS/EDC, Oracle InForm, REDCap or equivalent systems.

Direct experience supporting oncology clinical trials, biomarker-driven studies, companion diagnostics, precision medicine programs, or regulated IVD development strongly preferred.

Ability to interpret regulatory standards, guidance, and laws.

Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities.

Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments.

Experience working with external partners and/or regulatory bodies.

Knowledge of cancer diagnostics, Oncology and/or Pathology preferred.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 5, 2026 or until the job is no longer posted.

The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email [email protected] or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.

Travel Required:

Shift:

Day

Duration:

No End Date

Job Function:

Medical/Clinical

Apply Now

Refine Your Search

clinical data manager jobs in sacramento ca

Clinical Data Manager

Manager, Business Intelligence & Data Analytics

Clinical Supervisor (Licensed)

Clinical Research Program Manager

Clinical Research Coordinator II

Site Activation Manager

Senior Project Manager, Data Science Initiatives

Program Director

Applied AI Health Data Architect-Senior Manager

Mental Health Wraparound Program Supervisor - THRIVE FSP

Per Diem Clinical Research Nurse - Home Visits

Applied AI Health Data System Engineer-Senior Manager

Applied AI Health System Engineer – Senior Manager

Licensed Clinical Social Worker

ConvergeHEALTH - Commercial Life Sciences, Delivery Manager - Managed Platform as a Services (MPaaS) - Innovation_Delivery_Transformation

Clinical Team Lead Supervisor

Program Manager II/III, FIT Citrus Heights

Program Director Licensed - Hope Cooperative (TLCS, Inc.)

Clinical Manager

Clinical Team Supervisor

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