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Freelance Clinical Trials Data Analyst Jobs (NOW HIRING)

City of Hope

Clinical Trials Data Coord

Duarte, CA · On-site

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 ...

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 ...

Tempus

Junior Clinical Trials Data Specialist

$46K - $50K/yr

Review patient clinical records and use relevant data to determine clinical trial matches ... Experience in critically evaluating clinical trials. * Basic knowledge of generative AI. CHI: $46 ...

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 ...

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Freelance Clinical Trials Data Analyst information

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

As of Sep 1, 2026, the average hourly pay for freelance 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 does a freelance clinical trials data analyst do?

A Freelance Clinical Trials Data Analyst is responsible for managing, analyzing, and interpreting data collected during clinical research studies. They work independently or on a contract basis with pharmaceutical companies, research organizations, or healthcare institutions to ensure the accuracy, integrity, and compliance of clinical trial data. Their tasks often include cleaning datasets, running statistical analyses, generating reports, and helping researchers draw valid conclusions about the safety and efficacy of medical treatments. Freelancers in this role must be skilled in statistical software, understand regulatory requirements, and communicate findings clearly to stakeholders.

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

To excel as a Freelance Clinical Trials Data Analyst, you need a solid background in statistics, clinical research processes, and data management, usually supported by a degree in life sciences or a related field. Familiarity with statistical analysis software (such as SAS, R, or SPSS), clinical data management systems (CDMS), and relevant certifications like SAS certification or GCP (Good Clinical Practice) is highly valued. Strong attention to detail, problem-solving skills, and effective communication are crucial soft skills for interpreting data and collaborating with research teams. Mastering these skills ensures accurate data analysis, regulatory compliance, and successful clinical trial outcomes.

How do freelance clinical trials data analysts typically collaborate with research teams while working remotely?

Freelance Clinical Trials Data Analysts often work closely with cross-functional teams, such as clinical researchers, biostatisticians, and project managers, via virtual communication tools. Regular video conferences, shared databases, and secure data transfer platforms are commonly used to ensure smooth collaboration and data integrity. Clear documentation, prompt email communication, and proactive status updates are essential to stay aligned with study timelines and regulatory requirements. Building strong relationships with team members, even remotely, is key to successful project outcomes and ongoing opportunities.

What is the difference between Freelance Clinical Trials Data Analyst vs Clinical Data Coordinator?

AspectFreelance Clinical Trials Data Analyst
CredentialsTypically requires a degree in life sciences, statistics, or related fields; certifications like CDISC or SAS are common
Work EnvironmentRemote or freelance settings, project-based work for multiple clients
Employer/Industry UsageHired by CROs, pharmaceutical companies, or as independent consultants
Job FocusAnalyzing clinical trial data, statistical reporting, data validation

In contrast, a Clinical Data Coordinator usually works in a clinical setting, managing data entry and database management. While both roles require knowledge of clinical data, the freelance analyst focuses on data analysis and reporting, often working independently, whereas the coordinator handles data collection and quality control within a clinical trial team.

What cities are hiring for Freelance Clinical Trials Data Analyst jobs?

Cities with the most Freelance Clinical Trials Data Analyst job openings:

What are the most commonly searched types of Clinical Trials Data Analyst jobs?

The most popular types of Clinical Trials Data Analyst jobs are:

What states have the most Freelance Clinical Trials Data Analyst jobs?

States with the most job openings for Freelance Clinical Trials Data Analyst jobs include:

Freelance Clinical Trials Data Analyst jobs near you

Clinical Trials Data Coord

Duarte, CA • On-site

City of Hope
Hospitals • 1 - 5K employees

8.4

Company rating: 8.4 out of 10

Based on 91 frontline employees who took The Breakroom Quiz

25th of 896 rated healthcare providers

People enjoy working here

Good employer

Recommended by parents

Learn more about City of Hopeexternal

Full-time

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

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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