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Clinical Data Validation Jobs (NOW HIRING)

Carina Health Network

Clinical Data Engineer

Denver, CO · On-site

$85K - $100K/yr

Clinical Data Engineer - Remote, Must Live in State of Colorado Join Carina Health Network and help ... Develop data validation reports and analysis where applicable. * Develop technical documentation of ...

Carina Health Network

Clinical Data Engineer

Denver, CO · Remote

$85K - $100K/yr

Clinical Data Engineer - Remote, Must Live in State of Colorado Join Carina Health Network and help ... Develop data validation reports and analysis where applicable. * Develop technical documentation of ...

Carina Health Network

Clinical Data Engineer

Denver, CO · On-site

$85K - $100K/yr

Clinical Data Engineer - Remote, Must Live in State of Colorado Join Carina Health Network and help ... Develop data validation reports and analysis where applicable. * Develop technical documentation of ...

Ceribell, Inc

Clinical Data Manager

Sunnyvale, CA · On-site

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for ... Plan and manage UAT, ensuring systems are validated, functional, and audit-ready * Drive data ...

Ceribell, Inc

Clinical Data Manager

San Jose, CA · On-site

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for ... Plan and manage UAT, ensuring systems are validated, functional, and audit-ready * Drive data ...

Ceribell, Inc

Clinical Data Manager

Mountain View, CA

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for ... Plan and manage UAT, ensuring systems are validated, functional, and audit-ready * Drive data ...

Ceribell, Inc

Clinical Data Manager

Palo Alto, CA · On-site

$190K - $200K/yr

The Clinical Data Manager is the technical lead for clinical data management, accountable for ... Plan and manage UAT, ensuring systems are validated, functional, and audit-ready * Drive data ...

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$39

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How much do clinical data validation jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for clinical data validation in the United States is $39.26, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $51.92 per hour, depending on experience, location, and employer.

What is a Clinical Data Validation job?

A Clinical Data Validation job involves verifying and ensuring the accuracy, consistency, and integrity of clinical trial data. Professionals in this role check data for errors, discrepancies, and adherence to regulatory standards. They work closely with data management teams, using various validation tools and programming techniques to clean and validate data. This process ensures that clinical trial results are reliable and meet compliance requirements set by agencies like the FDA or EMA.

What are the typical day-to-day responsibilities of someone working in Clinical Data Validation?

In a Clinical Data Validation role, your daily tasks often include reviewing clinical trial data for accuracy and completeness, identifying and resolving discrepancies, and ensuring compliance with regulatory standards. You may work closely with data managers, biostatisticians, and clinical teams to address data queries and support ongoing data cleaning activities. Additionally, you’ll assist with the development and implementation of data validation plans, perform system checks, and contribute to the preparation of final study databases for analysis. These responsibilities require a high level of precision and a collaborative mindset, as quality data is crucial for the success of clinical research projects.

What are the key skills and qualifications needed to thrive in the Clinical Data Validation position, and why are they important?

To excel in Clinical Data Validation, a strong background in clinical research, data management, and attention to detail is crucial, often supported by a degree in life sciences or a related field. Familiarity with data validation software, electronic data capture (EDC) systems, and knowledge of regulatory compliance guidelines such as CDISC and GCP are typically required. Excellent analytical thinking, problem-solving skills, and clear communication are vital for collaborating with cross-functional teams. These competencies ensure the accuracy and reliability of clinical trial data, which is essential for regulatory approvals and successful study outcomes.

More about Clinical Data Validation jobs
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Clinical Data Validation jobs near you
Infographic showing various Clinical Data Validation job openings in the United States as of May 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $81,651 per year, or $39.3 per hour.
Clinical Data Manager (Contract)

Clinical Data Manager (Contract)

Adverum Biotechnologies, Inc.

Redwood City, CA • On-site

Contractor

Posted 25 days ago

Job description

Adverum Biotechnologies, Inc., a wholly owned subsidiary of Eli Lilly and Company is a mission-driven clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians' offices to eliminate the need for frequent ocular injections to treat these diseases. By overcoming the challenges associated with current treatment paradigms for these debilitating ocular diseases, Adverum aspires to transform the standard of care, preserve vision, and create a profound societal impact around the globe.
 
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 goals and objectives, including oversight of the CRO DM Vendor, if the project is outsourced. The CDM / Senior CDM will report to the Head of Clinical Data Management and will work closely with a cross-functional team in a fast-paced high growth environment team to ensure that clinical data are complete, high quality and delivered on time and budget.
 
This is a 6-12 month contract.  
 
Note to Recruiters and Agencies
All recruiter and agency inquiries must go through Adverum's internal Talent Acquisition team.  Unsolicited resumes sent to Adverum will be considered property of Adverum.   Agencies must be expressly engaged by Adverum's Talent Acquisition team for any requisition.  Direct contact with hiring managers by agencies will not be tolerated and may affect your ability to work with Adverum in the future.
What you'll do:
  • Responsible for compliance with regulatory and ICH guidelines, GCPs, company guidelines and Standard Operating Procedures, and CDM best practices.
  • Independently serves as the lead point of contact for all data management study-related communications.
  • Independently leads EDC development, including CRF development, EDC specification process, edit check development and User Acceptance Testing including test scripts and execution logs, issue logs, and UAT summary reports.
  • Reviews and assists in the development of study documents drafted by CROs such as Data Management Plans, Data Validation Specifications, eCRF Completion Guidelines, Data Review Plans, Data Transfer Agreements, and other cross-functional study documents that may require data management input.
  • Ensures the quality of clinical data within the EDC and other databases through regular data review and external data reconciliation processes and communicates any outstanding issues to the cross-functional teams.
  • Monitors and tracks the quality of all data management deliverables.
  • Leads data deliverables including snapshots for DMC, investor relations, publications, etc., and interim and final database locks, in collaboration with the CRO DM Vendor.
  • Effectively oversees contracted vendors, or vendor groups within CRO, to ensure data are complete, accurate and delivered within agreed on timelines.
  • Leads and facilitates Data Review Meetings with the cross-functional team, presenting metrics, trends, risks, and or issues.
  • Actively participates in team meetings - DM or cross-functional.
  • Coordinates transfers of SAS datasets or external data transfers from CROs.
  • Support TFL reviews, yearly regulatory submission requirements, compilation of CSRs, etc.
  • Responsible for TMF maintenance of data management-related study documents.
  • Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
About You:
  • Bachelor's degree or equivalent in life science, computer science, or related discipline.
  • 5+ years (CDM) / 8+ years (Sr. CDM) of experience working within a pharmaceutical or CRO environment, with experience in managing Phase I, II and/or III studies, from start-up through closure.
  • Demonstrated proficiency in various EDC Systems within the last 3 years.
  • Demonstrated proficiency in data management processes, clinical trial processes, and applicable regulatory requirements.
  • Good working knowledge of ICH, FDA, and GCP regulations and guidelines.
  • Experience with web-based Electronic Data Capture (EDC such as iMedidata Rave, Oracle InForm, etc.), clinical data management systems - eCOA, IRT, and industry wide thesauri, such as MedDRA and WHO Drug.
  • Experience in managing CRO Data Management vendors.
  • Knowledge of industry standards (CDISC, CDASH, SDTM, etc.).
  • Demonstrated proficiency in Microsoft Word, Project, PowerPoint, Office, and Excel.
  • Excellent organizational skills and attention to detail.
  • Effective communication (verbal/written) and interpersonal skills.
  • Able to set priorities and juggle multiple projects and demands.
  • Able to think critically and independently and be a proactive problem-solver.
  • Able to lead and work independently while exercising initiative, flexibility, and sound judgment.
  • Comfortable working in a fast-paced environment with different levels of the company including senior level management.
  • Proven ability to work both independently and in a team setting.
$70 - $85 an hour
This is a 6-12 month contract position.  The hourly rate is from $70-85 per hour, depending on the experience level.  
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