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 ...
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 ...
Clinical Data Associate
Foster City, CA · On-site
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 ...
Clinical Data Associate
Foster City, CA · On-site
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 ...
Clinical Data Associate III Duration: 6 Months Location: Foster City, CA 94404 Specific Responsibilities: This role will immediately assume biomarker data management responsibilities for representing ...
Clinical Data Associate III Duration: 6 Months Location: Foster City, CA 94404 Specific Responsibilities: This role will immediately assume biomarker data management responsibilities for representing ...
Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery. * Assists in the ...
Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery. * Assists in the ...
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 ...
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 ...
... clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. Demonstrate a general ...
... clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker data acquisition, quality checking and reporting. Demonstrate a general ...
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
Senior Clinical Data Manager
Redwood City, CA · On-site
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
Senior Clinical Data Manager
Redwood City, CA · On-site
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
Senior Clinical Data Manager
Redwood City, CA · On-site
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
Senior Clinical Data Manager
Redwood City, CA · On-site
This person may have project level oversight of junior data managers and/or Clinical Data Associates (CDAs). The core duties and responsibilities of the Sr/CDM are delineated below. Specifically, you ...
The Associate Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management ...
The Associate Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management ...
Associate Director, Clinical Data Management
$229K - $269K/yr
The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of ...
Associate Director, Clinical Data Management
$229K - $269K/yr
The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of ...
The Associate Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management ...
The Associate Director, Clinical Data Management, will be required to collaborate closely with other functional leaders to ensure clinical trial success. Defines project-level data management ...
Associate Director, Clinical Data Management
Redwood City, CA · On-site
$229K - $269K/yr
The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of ...
Associate Director, Clinical Data Management
Redwood City, CA · On-site
$229K - $269K/yr
The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of ...
Provide a high level of expertise in data management to support clinical studies. * Provide clear verbal or written information and hands-on support to project team members and to CROs related to ...
Provide a high level of expertise in data management to support clinical studies. * Provide clear verbal or written information and hands-on support to project team members and to CROs related to ...
Provide a high level of expertise in data management to support clinical studies. * Provide clear verbal or written information and hands-on support to project team members and to CROs related to ...
Provide a high level of expertise in data management to support clinical studies. * Provide clear verbal or written information and hands-on support to project team members and to CROs related to ...
Visual Analytics Associate Job ID: 7225733 Location:625 E Grand Ave, Escondido, CA 92025, USA ... Background in clinical data and/or clinical development Background in software development Working ...
Visual Analytics Associate Job ID: 7225733 Location:625 E Grand Ave, Escondido, CA 92025, USA ... Background in clinical data and/or clinical development Background in software development Working ...
Associate Director - Data Standards (Hybrid)
South San Francisco, CA · On-site
$141K/yr
Communication - Clearly communicates an understanding of clinical data standards concepts, clinical principles, and regulatory guidance and acts in accordance with those principles. Effectively ...
Associate Director - Data Standards (Hybrid)
South San Francisco, CA · On-site
$141K/yr
Communication - Clearly communicates an understanding of clinical data standards concepts, clinical principles, and regulatory guidance and acts in accordance with those principles. Effectively ...
Communication - Clearly communicates an understanding of clinical data standards concepts, clinical principles, and regulatory guidance and acts in accordance with those principles. Effectively ...
Quick apply
Communication - Clearly communicates an understanding of clinical data standards concepts, clinical principles, and regulatory guidance and acts in accordance with those principles. Effectively ...
... the Associate Chairs of Research and other stakeholders * Assist with the development and validation of PRISM reports related to the research mission. 15 YesThe Clinical Revenue and Research Data ...
... the Associate Chairs of Research and other stakeholders * Assist with the development and validation of PRISM reports related to the research mission. 15 YesThe Clinical Revenue and Research Data ...
Clinical Data Associate information
See Berkeley, CA salary details
$17.07 - $25.18
5% of jobs
$25.18 - $33.29
6% of jobs
$36.42 is the 25th percentile. Wages below this are outliers.
$33.29 - $41.39
35% of jobs
The median wage is $42.18 / hr.
$41.39 - $49.50
38% of jobs
$49.50 - $57.61
6% of jobs
$57.61 - $65.72
3% of jobs
$65.72 - $73.82
2% of jobs
$73.82 - $81.93
0% of jobs
$81.93 - $90.04
0% of jobs
$90.04 - $98.15
1% of jobs
$98.15 - $106.26
3% of jobs
$17
$47
$106
How much do clinical data associate jobs pay per hour?
What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?
What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?
What does a clinical data associate do?
What does a clinical data associate do?
A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.
What is the difference between Clinical Data Associate vs Clinical Research Coordinator?
| Aspect | Clinical Data Associate | Clinical Research Coordinator |
|---|---|---|
| Primary Role | Manage and ensure accuracy of clinical trial data | Oversee trial operations, patient recruitment, and site management |
| Credentials | Bachelor's in life sciences or related field; familiarity with data management | Bachelor's in health sciences or related field; clinical trial experience |
| Work Environment | Data management teams, clinical trial databases | Clinical sites, hospitals, research facilities |
| Industry Usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, clinical trial sites |
While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.
What are the most commonly searched types of Clinical Data jobs in Berkeley, CA?
The most popular types of Clinical Data jobs in Berkeley, CA are:
What are popular job titles related to Clinical Data Associate jobs in Berkeley, CA?
For Clinical Data Associate jobs in Berkeley, CA, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Berkeley, CA look for?
The top searched job categories for Clinical Data Associate jobs in Berkeley, CA are:
What cities near Berkeley, CA are hiring for Clinical Data Associate jobs?
Cities near Berkeley, CA with the most Clinical Data Associate job openings:

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