ZipRecruiter

Log In

1

Clinical Data Associate Jobs (NOW HIRING)

Penumbra

Clinical Data Analyst II

General Summary The Clinical Data Analyst II, under minimal supervision of the Associate Manager of Clinical Data Analytics or higher, selects the appropriate data sources and utilizes strong hands ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

Everest Clinical Research ("Everest") is a full-service, global, contract research organization ... Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data ...

Novartis

Clinical Data Engineering Lead

Cambridge, MA

$176K - $327K/yr

Novartis Biomedical Research (NBR) is searching for a visionary Associate Director to lead Clinical Data Engineering within our Oncology Data Science (OncDS) team. In this pivotal role, you'll be at ...

NYULMC

Research Data Associate

New York, NY · On-site

Inputs clinical and non-clinical data into the database and or case report forms. Extracts data for ... To qualify you must have a Associate's degree plus one year related experience or equivalent ...

Icon plc

Clinical Data Science Lead

Blue Bell, PA · Hybrid

OR associate's degree with at least 5 years' professional experience in clinical data management; OR High School Diploma (or equivalent) with at least 8 years' professional experience in clinical ...

next page

Showing results 1-20

All JobsClinical Data Associate Jobs

Clinical Data Associate information

See salary details

$13

$38

$86

How much do clinical data associate jobs pay per hour?

As of Jun 30, 2026, the average hourly pay for clinical data associate in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

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?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, 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.

More about Clinical Data Associate jobs
What cities are hiring for Clinical Data Associate jobs? Cities with the most Clinical Data Associate job openings:
What are the most commonly searched types of Clinical Data jobs? The most popular types of Clinical Data jobs are:
Who are the top companies hiring for Clinical Data Associate jobs? The top employers for Clinical Data Associate jobs are:
What states have the most Clinical Data Associate jobs? States with the most job openings for Clinical Data Associate jobs include:
What job categories do people searching Clinical Data Associate jobs look for? The top searched job categories for Clinical Data Associate jobs are:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 1% Temporary, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.
Clinical Data Review Associate - Oncology/Hematology

Clinical Data Review Associate - Oncology/Hematology

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, PTO

Posted yesterday

Key responsibilities

  • Perform comprehensive manual review of clinical data collected in trials.

  • Develop clinical review guidelines for specific therapeutic areas.

  • Interface with the Data Management team to assure query resolution.

Medpace rating

8.5

Company rating: 8.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

12th of 58 rated research

Job description

Job Summary
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Reviewer to join our Clinical Coding & Support team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous nursing expertise and can develop and grow your career even further, then this is the opportunity for you!
Responsibilities
  • Comprehensive manual review of clinical data collected in trials;
  • Development of clinical review guidelines for specific therapeutic areas;
  • Interface with Data Management team to assure query resolution.
  • Seeking specialization in following therapeutic areas:
    • Oncology
    • Infectious Disease
    • Cardiology
    • Endocrine
    • Hematology

*Stable schedule with no weekends, no work on Medpace holidays, and flexible work schedule*
Qualifications
  • Bachelor's of Science in Nursing and RN required,
  • At least 3-4 years of nursing experience
  • 1-2 years of specific therapeutic experience
  • General knowledge of clinical trial processes and/or experience working with clinical data; and
  • Familiarity with Microsoft Excel preferred.

TRAVEL: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards
  • Named a Top Workplace in 2024 by The Cincinnati Enquirer
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Medpace logo

About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

View All Medpace Jobs

Apply