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Senior Clinical Trials Data Analyst Jobs (NOW HIRING)

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.

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.

The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning ... Trials, Data Analysis, Decision Making, Drug Development, Early Clinical Development, Ethical ...

Sr. Clinical Trials Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ... Uses gained experience to give high level analyses of study data * Reviews and Monitors Clinical ...

Sr. Clinical Trials Associate

Aliso Viejo, CA

$35.50 - $48.50/hr

The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ... Uses gained experience to give high level analyses of study data * Reviews and Monitors Clinical ...

Sr. Clinical Trials Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ... Uses gained experience to give high level analyses of study data * Reviews and Monitors Clinical ...

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Senior Clinical Trials Data Analyst information

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

As of Aug 3, 2026, the average hourly pay for senior clinical trials data analyst in the United States is $42.60, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $48.08 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Clinical Trials Data Analyst jobs? The most popular types of Clinical Trials Data Analyst jobs are:

Sr Clinical Trials Data Coord

City of Hope

Duarte, CA

Other

Posted 6 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

26th 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. 

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 query resolution to ensure accurate, reliable, and compliant research data. The role involves interpreting research protocols, reviewing medical records, resolving discrepancies, and maintaining study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems. Working closely with physicians, clinical coordinators, and research teams, the coordinator ensures timely data reporting, supports adverse event data collection, and contributes to study monitoring and regulatory compliance. Additionally, the role includes performing peer data reviews, assisting in the development of data management plans and workflows, and providing training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations.

As a successful candidate, you will: 

  • Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout.
  • Ensure data accuracy, completeness, and compliance through quality checks, data cleaning, and timely resolution of queries.
  • Maintain regulatory compliance with FDA, ICH-GCP, ALCOA , HIPAA, and other applicable guidelines for clinical research data management.
  • Collaborate with sponsors, physicians, and clinical coordinators to resolve protocol issues, data discrepancies, and ensure proper documentation.
  • Manage adverse event documentation and classification using standard dictionaries such as MedDRA, CTCAE, and WHO-DDE, including SAE follow-up and query resolution.
  • Maintain study calendars, financial triggers, and data completion tracking in CTMS to support billing and study financial management.
  • Support monitoring visits, study initiation visits, audits, and inspection readiness, ensuring data quality and completeness.
  • Contribute to data management improvements by assisting with EDC builds, creating data standards, preparing reports, participating in CAPA and process improvement initiatives, and mentoring peers.
 
Qualifications - External
 
Qualifications - External

Your qualifications should include: 

Minimum Education

 Bachelor's degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience.

Minimum Experience: Minimum of 5-7 years of clinical research or related experience.

Required Certifications:

 Completion of Good Clinical Practice (GCP) training within 1 month of employment.

 Completion of Human Subjects Protection (HSP) training within 1 month of employment.

Ability to obtain SOCRA or ACRP certification within 2 years of employment.
Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems.

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 commitment to diversity, equity, and inclusion, please click here.

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