1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) ...
Qualifications Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience Understanding of clinical data management processes Project management experience of clinical trials ...
Qualifications Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience Understanding of clinical data management processes Project management experience of clinical trials ...
Clinical Data Manager
Milpitas, CA · On-site
Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...
Clinical Data Manager
Milpitas, CA · On-site
Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...
Clinical Data Manager
Milpitas, CA · On-site
Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...
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Clinical Data Manager
Milpitas, CA · On-site
Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...
Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...
Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management, quality control, and analysis of clinical cohort data. This role ensures data integrity, identifies and ...
Provide clinical data management support for study operations and analysis groups * including the following. * Assist in defining and creation of data listings, including programming software to ...
Provide clinical data management support for study operations and analysis groups * including the following. * Assist in defining and creation of data listings, including programming software to ...
Provide clinical data management support for study operations and analysis groups * including the following. * Assist in defining and creation of data listings, including programming software to ...
Provide clinical data management support for study operations and analysis groups * including the following. * Assist in defining and creation of data listings, including programming software to ...
Clinical Data Manager
Sunnyvale, CA · On-site +1
Provide clinical data management support for study operations and analysis groups * including the following. * Assist in defining and creation of data listings, including programming software to ...
Clinical Data Manager
Sunnyvale, CA · On-site +1
Provide clinical data management support for study operations and analysis groups * including the following. * Assist in defining and creation of data listings, including programming software to ...
Senior Clinical Data Manager
Redwood City, CA · On-site
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
Senior Clinical Data Manager
Redwood City, CA · On-site
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
The Senior Clinical Data Manager is responsible for all aspects of the data management process from the development of project documentation, system set-up, User Acceptance Testing (UAT), routine ...
The Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team ...
The Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team ...
Senior Clinical Data Manager
Emeryville, CA · On-site
Experience with Electronic Data Capture (EDC) * Excellent verbal and written communication skills and strong interpersonal skills * Experience managing Clinical Research Organizations (CROs)
Senior Clinical Data Manager
Emeryville, CA · On-site
Experience with Electronic Data Capture (EDC) * Excellent verbal and written communication skills and strong interpersonal skills * Experience managing Clinical Research Organizations (CROs)
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) ...
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience 2) Project management experience of clinical trials 3) Understanding of clinical data management processes 4) ...
Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience Project management experience of clinical trials Understanding of clinical data management processes Communication ...
Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience Project management experience of clinical trials Understanding of clinical data management processes Communication ...
The Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management strategy.
The Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management strategy.
Clinical Data Associate III Duration: 6 Months Location: Foster City, CA 94404 Specific ... This role will immediately assume biomarker data management responsibilities for representing ...
Clinical Data Associate III Duration: 6 Months Location: Foster City, CA 94404 Specific ... This role will immediately assume biomarker data management responsibilities for representing ...
The Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management strategy.
The Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management strategy.
The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:
The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Clinical Data Manager information
See San Ramon, CA salary details
$22.30 - $28.60
4% of jobs
$28.60 - $34.90
10% of jobs
$34.90 - $41.20
2% of jobs
$41.20 - $47.50
4% of jobs
$50.65 is the 25th percentile. Wages below this are outliers.
$47.50 - $53.80
9% of jobs
$53.80 - $60.10
10% of jobs
The median wage is $65.35 / hr.
$60.10 - $66.40
13% of jobs
$66.40 - $72.70
17% of jobs
$74.56 is the 75th percentile. Wages above this are outliers.
$72.70 - $79
18% of jobs
$79 - $85.30
7% of jobs
$85.30 - $91.60
5% of jobs
$22
$63
$91
How much do clinical data manager jobs pay per hour?
What are some common challenges clinical data managers face when working on multi-site clinical trials?
What are the key skills and qualifications needed to thrive as a clinical data manager?
What does a clinical data manager do?
What does a clinical data manager do?
A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).
- What is the career path for a clinical data manager?
- What is the salary of a clinical data manager?
- What is the difference between a clinical data scientist and a clinical data manager?
- How to become a clinical data manager?
- What Is a Clinical Data Manager and How to Become One
- Clinical Data Manager Job Description Sample Template

Job description
1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience
2) Project management experience of clinical trials
3) Understanding of clinical data management processes
4) Communication with cross-functional study team members
Specific Responsibilities:
- This role will immediately assume biomarker data management responsibilities for representing biomarker data management at the biomarker Sub Team (BST) meetings. The candidate will also be responsible for providing oversight to studies that fall within the BSTs.
- The selected candidate will manage biomarker data in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high level of data quality by leveraging and adhering to standard data structures and corresponding standard edit checks and review listings.
- The selected candidate may also manage and lead in the design and implementation of biomarker data management processes with vendors, ensuring completeness, correctness, and consistency according to the Client's standards.
- This role has a high degree of collaboration with the Biomarker cross-functional team members, study team members and other biomarker Clinical Data Associates.
The ideal candidate should possess a BS degree or higher in a Biomedical Science or equivalent and minimum 3 years of relevant clinical data management experience and preferably along with biomarker or laboratory background and experience in a CRO or bio/pharmaceutical setting.
- Essential Duties and Job Functions:
- Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Biobanking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting.
- Demonstrates a general understanding of each assigned protocol, critical tasks and milestones.
- Ensure completeness, correctness and consistency of routine clinical data and data structure.
- Responsibilities include: assisting in the developing the data transfer specifications, the data mapping specifications, the data quality review plan and the data validation specifications, vendor management, data review and data reconciliation. Assists in implementing routine clinical research projects and standards.
- Identifies, tracks, and resolves routine queries. Utilizes routine reports to track study progress and ensures timeliness and quality expectations are met.
- Knowledge, Experience and Skills: 3 years of experience and a BS degree.
- 1 years of experience and a MS degree or PhD.
All your information will be kept confidential according to EEO guidelines.
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996