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Senior Clinical Data Associate Jobs (NOW HIRING)

Clover Health

Senior Clinical Data Analyst

As a Senior Clinical Data Analyst in the Clover Care Services (CCS) organization, you will help drive better patient outcomes, improve care coordination, and optimize resource utilization by ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...

ImmunityBio, Inc.

Senior Clinical Data Manager

Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...

Danaher

Senior Clinical Data Manager

Vista, CA · On-site +1

Responsible for all activities of clinical trial data management including CRF design, database and ... including senior leaders * Excellent organizational skills and ambition to continuously improve ...

Danaher

Senior Clinical Data Manager

New York, NY · On-site +1

Responsible for all activities of clinical trial data management including CRF design, database and ... including senior leaders * Excellent organizational skills and ambition to continuously improve ...

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How much do senior clinical data associate jobs pay per year?

As of Jul 6, 2026, the average yearly pay for senior clinical data associate in the United States is $58,937.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,000.00 and $67,500.00 per year, depending on experience, location, and employer.

What are some common challenges Senior Clinical Data Associates face when managing large clinical trial datasets?

Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.

What are the key skills and qualifications needed to thrive as a Senior Clinical Data Associate, and why are they important?

To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.

What does a Senior Clinical Data Associate do?

A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.
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What are the most commonly searched types of Senior Clinical Data jobs? The most popular types of Senior Clinical Data jobs are:
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Senior Clinical Data Associate jobs near you
Clinical data Manager

Clinical data Manager

Integrated Resources INC

Foster City, CA • On-site

Contractor

Posted 3 days ago

Job description

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.
Additional Information

All your information will be kept confidential according to EEO guidelines.

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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

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