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Clinical Data Jobs (NOW HIRING)

University of Utah

Clinical Data Managers

Salt Lake City, UT · On-site

$34.77K - $84.20K/yr

Build, review, and maintain clinical databases, data collection tools, and applications. Create, review, and maintain study documentation, such as Case Report Forms (CRFs), Data Management Plans (DMP ...

Lilly

Clinical Data Associate

Indianapolis, IN

The Clinical Data Associate is accountable for the end-to-end clinical data sciences delivery for a clinical study, including clinical database build, data acquisition, storage, retrieval, and ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

Details Open Date 03/26/2026 Requisition Number PRN44567B Job Title Clinical Data Managers Working Title Clinical Data Manager Career Progression Track P00 Track Level P3 - Career, P2 - Developing ...

University of Utah

Clinical Data Managers

Salt Lake City, UT · On-site +1

$50.91K - $69.59K/yr

Details Open Date 03/26/2026 Requisition Number PRN44567B Job Title Clinical Data Managers Working Title Clinical Data Manager Career Progression Track P00 Track Level P3 - Career, P2 - Developing ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

Details Open Date 03/26/2026 Requisition Number PRN44567B Job Title Clinical Data Managers Working Title Clinical Data Manager Career Progression Track P00 Track Level P3 - Career, P2 - Developing ...

Sumitomopharma

OR

$130.40K - $163K/yr

This position reports to the Executive Director, Clinical Data Management, Oncology and is part of the Oncology Data Management function, which supports Sumitomo Pharma America's clinical development ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Support clinical data review requirements from Lead data manager. * Create customise data review listings for study per specifications from lead data manager. * Provide clinical data management ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50.91K - $69.59K/yr

Details Open Date 03/26/2026 Requisition Number PRN44567B Job Title Clinical Data Managers Working Title Clinical Data Manager Career Progression Track P00 Track Level P3 - Career, P2 - Developing ...

Belcan

Clinical Data Manager

Durham, NC · On-site

$55 - $65/hr

Clinical Data Manager Location: Durham, NC Duration: 09 Months contract(Potential temp to Perm) Payrate: $55/hr. - $65/hr. (Depending on experience) Shift: 1st shift, Mon-Fri , 8am-4:30pm Start Date:

R3tek

Clinical Data Analyst

Hillsborough, NJ · On-site

R3 Technology Inc. seeks Clinical Data Analyst for it Hillsborough NJ office. Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on ...

R3TEK

Clinical Data Analyst

Hillsborough, NJ

R3 Technology Inc. seeks Clinical Data Analyst for it Hillsborough NJ office. Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on ...

Sumitomo Pharma

Clinical Data Manager

$130.40K - $163K/yr

This position reports to the Executive Director, Clinical Data Management, Oncology and is part of the Oncology Data Management function, which supports Sumitomo Pharma America's clinical development ...

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Clinical Data information

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$19

$57

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How much do clinical data jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical data in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Data Specialist, you need a solid background in life sciences, data management principles, and familiarity with regulatory guidelines, often supported by a relevant degree. Proficiency in clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of standards like CDISC or MedDRA is typically required. Strong attention to detail, analytical thinking, and effective communication skills are crucial soft skills for this role. These competencies ensure the accuracy and integrity of clinical trial data, supporting regulatory compliance and reliable outcomes in clinical research.

What are some of the common challenges faced by professionals working in Clinical Data roles, and how can they be addressed?

Professionals in Clinical Data roles often encounter challenges such as managing large volumes of complex data, ensuring data quality and integrity, and adhering to strict regulatory standards. These challenges can be addressed by staying updated on industry best practices, utilizing advanced data management tools, and working closely with cross-functional teams such as clinical research and regulatory affairs. Continuous professional development and effective communication within the team are also key to overcoming these hurdles and ensuring successful clinical trial outcomes.

What are clinical data?

Clinical data refers to information collected during the course of ongoing patient care or as part of a clinical trial program. This data includes patient demographics, medical history, lab results, imaging studies, treatment plans, and outcomes. Clinical data is crucial for informing medical decisions, improving patient care, and supporting medical research and drug development. It is typically collected and managed by healthcare providers, researchers, and data professionals while maintaining strict standards for patient privacy and data security.

What is the difference between Clinical Data vs Clinical Data Coordinator?

AspectClinical DataClinical Data Coordinator
CredentialsTypically requires a degree in health informatics, life sciences, or related fieldRequires similar credentials, often with additional certification in clinical research or data management
Work EnvironmentData analysis, database management, and reporting in healthcare or research settingsOversees data collection, entry, and quality control in clinical trial or healthcare environments
Employer & Industry UsageUsed across hospitals, research institutions, and pharmaceutical companiesCommonly employed in clinical research organizations and hospitals

While both roles involve handling clinical data, Clinical Data professionals focus on data analysis and management, whereas Clinical Data Coordinators oversee data collection and quality assurance in clinical trials or healthcare settings.

More about Clinical Data jobs
What cities are hiring for Clinical Data jobs? Cities with the most Clinical Data job openings:
What are the most commonly searched types of Clinical Data jobs? The most popular types of Clinical Data jobs are:
What states have the most Clinical Data jobs? States with the most job openings for Clinical Data jobs include:
What job categories do people searching Clinical Data jobs look for? The top searched job categories for Clinical Data jobs are:
Clinical Data jobs near you
Infographic showing various Clinical Data job openings in the United States as of May 2026, with employment types broken down into 3% As Needed, 72% Full Time, 19% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.
Clinical Data Manager/Clinical Data Reviewer

Clinical Data Manager/Clinical Data Reviewer

Charles River Laboratories

Manhattan, NY • Remote

Full-time

Medical, Vision, Retirement

This job post has expired today. Applications are no longer accepted.

Charles River Laboratories rating

8.1

Company rating: 8.1 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

31st of 70 rated pharmaceutical

Job description

Clinical Data Manager/Clinical Data Reviewer Join to apply for the Clinical Data Manager/Clinical Data Reviewer role at Charles River Laboratories For 75+ years, Charles River has advanced the discovery, development, and safe manufacture of new drug therapies. Join a global team where your expertise directly supports healthier lives worldwide. We are seeking an experienced Clinical Data Manager/Clinical Data Reviewer to join our Safety Assessment business on a full-time, permanent, remote basis (UK or EU).

In this role, you'll support end-to-end clinical data management processes, ensure data integrity, and collaborate closely with clients across multiple complex studies. Clinical Data Management & Transfer Prepare and review Data Transfer Agreements for all assay data types. Build strong client relationships through regular meetings and data presentations.

Create and QC SDTM and non-SDTM datasets . Ensure all datasets meet regulatory standards and are delivered securely. Use approved data exchange platforms for compliant data transfers.

Data Review & Quality Review clinical trial data for accuracy, completeness, and protocol adherence. Validate data coding, interpretation, and consistency. Conduct robust QC checks across all study documentation and regulatory requirements.

Partner with internal teams and external clients throughout the data lifecycle. Mentor and support peers; serve as team lead when applicable (Manager level). Host and participate in internal/external meetings to maintain project alignment.

Process Improvement Develop and maintain templates, tools, and SOPs. Lead or support initiatives focused on data automation and workflow enhancement (Manager level). What You Bring Education Bachelor's degree in a scientific discipline (preferred).

Experience Strong background in a research or pharmaceutical environment with hands‐on clinical data management and clinical data review experience. CRO/Pharma industry experience preferred. Comfortable in customer‐facing roles; able to build and maintain strong stakeholder relationships.

Technical Skills Knowledge of CDISC standards (CDASH, SDTM, Controlled Terminology). Experience with common data formats (.xml, .xpt, sas7bdat, ASCII, .DAT, .xlsx). Proficiency in Microsoft Office; able to learn validated systems quickly.

Soft Skills Excellent communication, organizational, and leadership abilities. Ability to manage complex workloads under tight timelines. At Manager level: exceptional customer service and relationship‐building skills.

If you're passionate about data integrity, collaboration, and advancing global health, we'd love to hear from you. Apply today and make an impact with Charles River. Seniority level Mid‐Senior level Employment type Full-time Job function Science Benefits Medical insurance Vision insurance 401(k) Pension plan Paid paternity leave #J-18808-Ljbffr

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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