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Clinical Trials Data Analyst Jobs (NOW HIRING)

City of Hope

Clinical Trials Data Coord

Duarte, CA

This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

City of Hope

Clinical Trials Data Coord

Duarte, CA

This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

City of Hope

Sr Clinical Trials Data Coord

Duarte, CA · On-site

The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and ...

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ...

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ...

PSRTEK

Clinical Data Analyst-REMOTE

New York, NY · On-site

Position: Clinical Data Analyst Location: - Remote(CST working hours) Experience: -10+ Years ... Prioritize clinical trials and assess opportunities for content expansion (e.g., biomarkers, prior ...

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · Remote

$70K - $85K/yr

... a Clinical Trials Coverage Analyst in a fully remote capacity, supporting a leading academic ... Proficiency in document and data management tools, including Microsoft Word, Excel, PowerPoint ...

EDJ Associates,

Protocol Data Analyst I

Washington, DC · On-site

Protocol Data Analyst I Department: Research Employment Type: Full Time Location: National Institue ... This role codes clinical trials using the NCI Thesaurus, abstracts biomarkers, processes accrual ...

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Clinical Trials Data Analyst information

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How much do clinical trials data analyst jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for clinical trials data analyst in the United States is $36.36, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $42.07 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trials data analyst?

To thrive as a Clinical Trials Data Analyst, you need strong analytical abilities, a solid understanding of biostatistics, knowledge of clinical trial processes, and a relevant degree in life sciences, statistics, or a related field. Familiarity with statistical programming languages like SAS or R, experience using clinical data management systems (such as Medidata or Oracle Clinical), and certifications like SAS Certified Clinical Trials Programmer are highly valuable. Excellent attention to detail, problem-solving skills, and the ability to collaborate effectively with cross-functional teams are important soft skills. These qualifications ensure accurate data analysis, regulatory compliance, and effective communication of findings, all vital to advancing clinical research outcomes.

What is a clinical trials data analyst?

A Clinical Trials Data Analyst is responsible for collecting, processing, and analyzing data from clinical studies to ensure accuracy, compliance, and statistical validity. They work with clinical researchers, data managers, and regulatory teams to interpret trends, validate findings, and report results. Their role is crucial for ensuring that clinical trial data meets regulatory standards and provides meaningful insights for drug development or medical research. Strong skills in statistical analysis, database management, and regulatory compliance are essential for this role.

What are the typical daily tasks and team interactions for a clinical trials data analyst?

As a Clinical Trials Data Analyst, your daily responsibilities often include cleaning and validating clinical data, performing statistical analyses, and generating reports or visualizations for study teams. You will closely collaborate with clinical researchers, data managers, statisticians, and project managers to ensure data integrity and address study objectives. Regular participation in team meetings, updates with cross-functional departments, and presenting analysis results are also common parts of the role. This teamwork is essential for successfully running clinical trials and delivering reliable insights to support regulatory submissions and medical advancements.

How to become a clinical trials data analyst?

To become a clinical trials data analyst, typically a bachelor's degree in a related field such as biology, statistics, or health sciences is required. Developing skills in data management, statistical software (like SAS or R), and understanding clinical trial processes are essential. Gaining experience through internships or entry-level roles in healthcare or research settings can also improve job prospects.
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Clinical Trials Data Analyst jobs near you
Infographic showing various Clinical Trials Data Analyst job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 88% Full Time, 6% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 7% Hybrid, and 10% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.

Clinical Trials Data Coord

City of Hope

Duarte, CA

Full-time

Re-posted 3 days ago

City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

25th of 887 rated healthcare providers

Job description

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. 
This full-time remote position entails ensuring data integrity for various research studies.  Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data.  You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research.
As a successful candidate, you will: 
  • Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations.
  • Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information.
  • Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution.
  • Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements.
  • Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work.
Qualifications - External
Qualifications - External
Qualifications - External
Qualifications - External
Qualifications - External

Your qualifications should include: 

  • Bachelor’s Degree, relevant experience may substitute for degree.
  • At least two years of experience related to the conduct of oncology clinical trials.
  • Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.

To learn more about our Comprehensive Benefits, please CLICK HERE.

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About City of Hope

Sourced by ZipRecruiter

City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Duarte, CA, US

Year founded

1913

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