Top 154 Clinical data manager Jobs in San Ramon Ca

Lead Clinical Data Manager
CooperVision —San Ramon, CA
- $164,819 - $219,758 a year
- Full-time
- Computer Science
- 5 years
- System design
Clinical Data Manager
CliniOps —Fremont, CA
- Mid-level
- Windows
- Analysis skills
Clinical Affairs Associate Manager
Rodan and Fields Beauty, LLC —San Ramon, CA
- $84,000 - $105,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- 5 years
Clinical Research, Associate I
Abbott Laboratories —Alameda, CA
- $73,900 - $116,000 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Communication skills
- Health insurance
- Tuition reimbursement
3d
Manager, Clinical Data Management
Alimentiv —San Francisco, CA
- $99,500 - $160,000 a year
- Full-time
- Remote
- 7 years
- Mentoring
- Recruiting
- Health insurance
- Dental insurance
Quick Apply
5d
Senior Manager, Clinical Data Management
Corcept Therapeutics —Redwood City, CA
- $170,550 - $200,700 a year
- Computer science
- Computer Science
- 5 years
Quick Apply
Clinical Trial Manager/Sr Clinical Trial Manager
Erasca —South San Francisco, CA
- $145,000 - $190,000 a year
- Remote
- Medicine
- Inventory management
- 5 years
- Health savings account
- AD&D insurance
Clinical Case Management and Wellness Counselor (Korean, ASW) (1.0 FTE)
Korean Community Center of the East Bay —San Leandro, CA
- $75,000 - $80,000 a year
- Email
- Hybrid work
- Background check
- School experience
- Clean driving record
- Wellness program
- Health savings account
Quick Apply
IOP Therapist
OCD Anxiety Centers —San Mateo, CA
- $75,000 - $100,000 a year
- Full-time
- Mid-level
- 2 years
- Communication skills
- Paid training
- Continuing education credits
Quick Apply
Clinician - Head of Service
Lighthouse Mentoring Center —Pittsburg, CA
- $80,000 - $90,000 a year
- 8 hour shift
- LMFT
- CPR Certification
- Current TB test
- Health insurance
- Dental insurance
Quick Apply
Senior AI ML Engineer - Remote
UnitedHealth Group —San Francisco, CA
- $120,100 - $214,500 a year
- Full-time
- Hybrid work
- Azure
- Computer Science
- Pass drug screening
AI Engineer
David Joseph & Company —San Francisco, CA
- $150,000 - $250,000 a year
- Full-time
- Remote
- HIPAA
- Mid-level
- 2 years
Quick Apply
Senior Clinical Program Manager
Arcus Biosciences —Hayward, CA
- $175,000 - $190,000 a year
- Full-time
- 7 years
- Office
- Analysis skills
1d
Manager, Population Health Analysis - 26-06
PriMed Management Consulting Services, Inc. —San Ramon, CA
- $134,000 - $179,000 a year
- Full-time
- 3 years
- Master's degree
- SQL
Quick Apply
Clinical Data Management Manager
Gilead Sciences —Foster City, CA
- $136,340 - $176,440 a year
- Full-time
- Master's degree
- Databases
- Bachelor's degree
- Health insurance
- Dental insurance
Clinical Trials Manager, Early Phase Oncology (Office Based)
Gilead Sciences —Foster City, CA
- $133,195 - $189,640 a year
- Full-time
- Mid-level
- Office
- Master's degree
- Health insurance
- Dental insurance
Senior Clinical Trial Manager
Neurocentria —Walnut Creek, CA
- $160,000 - $190,000 a year
- Full-time
- Hybrid work
- Nursing
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Quick Apply
Clinical Data Manager
AccuScan Sciences —Milpitas, CA
- Full-time
- Hybrid work
- 3 years
- SQL
- Analysis skills
Quick Apply
13d
Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)
AbbVie —South San Francisco, CA
- $109,500 - $208,500 a year
- Full-time
- Hybrid work
- Bachelor of Science
- 8 years
- Analysis skills
- Paid holidays
- Health insurance
7d
Manager, Clinical Operations
iota Biosciences, Inc. —Alameda, CA
- $145,000 - $200,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Mentoring
- Senior level
- Paid parental leave
- Health insurance
14d

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Lead Clinical Data Manager

CooperVision -
San Ramon, CA

Apply Now

Job Details

Full-time
$164,819 - $219,758 a year

Qualifications

Vendor relationship building

Full Job Description

At CooperVision, a division of CooperCompanies, we’re driven by a unifying purpose to help people to experience life’s beautiful moments. We are connected through our shared values - dedicated, innovative, friendly, partners, and do the right thing. As a leading global manufacturer of contact lenses, we are committed to helping improve the way people see each day. Through our diverse lens portfolio, we tackle the toughest vision challenges – including astigmatism, presbyopia, and childhood myopia. We offer the most complete collection of spherical, toric, and multifocal products available, enabling us to fit 99% of all contact wearers. Learn more at www.coopervision.com.

This role is not eligible for employer-sponsored work authorization now or in the future. Applicants must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.)
This position requires full-time onsite work (5 days per week) in San Ramon, CA and is not eligible for relocation assistance.

Job Summary:

Leads all aspects of clinical data management activities from study initiation through database lock and study closeout. Develops, optimizes and controls data management system, including external clinical research centers in compliance with medical device regulations. Oversees and ensure that all CooperVision sponsored clinical trial data are accurate, complete, and compliant.

This role is not eligible for employer-sponsored work authorization now or in the future. Applicants must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.)
This position requires full-time onsite work (5 days per week) in our San Ramon, CA. office and is not eligible for relocation assistance.

Responsible for Clinical Data Management oversight for CooperVision sponsored clinical trials. Oversees the entire lifecycle of clinical trial data from setting up the database, data collection, and data dissemination for analysis and reporting, ensuring data quality, integrity, and compliance of databases, while adhering to strict regulatory and international standards under Good Clinical Practice to ensure patients’ safety and play a crucial part in Helping People Experience Life’s Beautiful Moments.

Knowledge, Skills and Abilities:

Bachelor’s degree in life science, computer science or closely related discipline plus minimum of 8 years of experience in Clinical Data Management, or
Master of Science in life science, computer science or closely related discipline plus minimum of 5 years of experience in Clinical Data Management
Highly dependable, good time management and multitasking skillsets
Proficiency with common electronic data capture (EDC) and clinical data management platforms, and clinical data systems (e.g., REDCap, Medrio, Medidata RAVE, Veeva).
Expertise in database design, validation, and oversight of external data integration.
Expert in the use of SQL to query datasets.
Passion for exploring and adopting emerging technologies, including AI-enabled tools, to support innovation, operational excellence, and business transformation
Strong problem-solving ability to navigate complex unforeseen situations
Strong leadership skillsets to guide and mentor within and cross-functional team members
Strong on written and verbal communications
Experience with integrating data from external vendors or systems.
Familiarity with statistical or visualization tools such as SAS or R is preferred.

Work Environment:

On-site 5 days a week in-office required
Normal office environment and ophthalmic clinical exam room
Sedentary to light physical effort necessary to perform the job.
Extensive contact with employees and external researchers

For U.S. locations that require disclosure of compensation, the starting base pay for this role is between $164,819.00 and $219,758.00. per year and may include cost of living adjustments. The actual base pay includes many factors and is subject to change and modification in the future. This position may also be eligible for other types of compensation and benefits.

We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.

#LI-SD1

Generate, contribute, and/or review key study documentation such as data management plans, case report forms (CRFs), database specifications, test plans for user acceptance testing (UAT), and data transfer specification and agreements
Lead electronic case report form (eCRF) developments and facilitate cross-functional reviews of eCRF content
Support the design, development, and validation of clinical trial databases and eCRFs, including edit checks within the Electronic Data Capture (EDC) system
Perform training on the EDC system, dataflow, and quality control (QC) processes to personnel as appropriate
Perform and/or oversee data cleaning, issue queries, query resolution, and delivery of high-quality datasets to support trial milestones and regulatory submissions; assist Clinical Operations, Biostatistics, Statistical Programming, Investigational sites, and/or Clinical Research Organization with resolving queries
Perform third party non-Case Report Form data management activities
Ensure delivery of datasets, annotated CRFs, and related materials in the appropriate formats
Participate in the preparation, review, and validation of submission-ready datasets for regulatory filings (e.g., FDA, EU MDR, PMDA, NMPA).
Lead efforts in developing and maintaining standard database validation checks for common modules as well as for indication or research objective specific modules
Ensure that documentation and data records, including archiving, meet regulatory and inspection standards
Ensure compliance with industry standards and regulations (ISO, FDA, EU MDR) and assist in audit and inspection readiness
Champion and assist the effective utilization of AI tools to enable automation, continuous process improvements, technology modernization, and efficiency initiatives.
Serve as the main liaison for vendors or partners handling data deliverables, clarifying expectations and maintaining streamlined communication between internal and external teams
Develop and/or modify standard operating procedures (SOPs) for clinical data management to comply with industry standards and regulations
Establish and manage data quality standards, ensuring adherence to internal procedures and external guidelines
Perform importing and reconciling external datasets, maintaining consistency across all study databases
Track and communicate progress metrics, risks, and outcomes to senior management

Travel Requirements:
Minimal travel (5%) required, occasionally to research centers to establish or improve data management procedures.

Apply Now

Refine Your Search

clinical data manager jobs in san ramon ca

Lead Clinical Data Manager

Clinical Data Manager

Clinical Affairs Associate Manager

Clinical Research, Associate I

Manager, Clinical Data Management

Senior Manager, Clinical Data Management

Clinical Trial Manager/Sr Clinical Trial Manager

Clinical Case Management and Wellness Counselor (Korean, ASW) (1.0 FTE)

IOP Therapist

Clinician - Head of Service

Senior AI ML Engineer - Remote

AI Engineer

Senior Clinical Program Manager

Manager, Population Health Analysis - 26-06

Clinical Data Management Manager

Clinical Trials Manager, Early Phase Oncology (Office Based)

Senior Clinical Trial Manager

Clinical Data Manager

Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)

Manager, Clinical Operations

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