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Remote Clinical Trials Data Analyst Jobs (NOW HIRING)

CG Oncology, Inc.

Senior Clinical Trials Scientist

$150K - $170K/yr

... data analysis, and reporting. The ideal candidate is a seasoned professional with demonstrated ... Remote Essential Functions * Provide scientific leadership for the planning, design, and ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · Remote

$125K - $175K/yr

... active clinical trials. This individual will play a critical role in ensuring high-quality ... Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · Remote

$125K - $175K/yr

... active clinical trials. This individual will play a critical role in ensuring high-quality ... Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ...

Cogstate

Project Manager, Clinical Trials

Our global team of experts - spanning psychology, data science, operations, and technology - works ... With supervision, analyze reports for project hours and budget utilization and making course ...

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Remote Clinical Trials Data Analyst information

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

As of Jun 23, 2026, the average hourly pay for remote 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 is the difference between Remote Clinical Trials Data Analyst vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trials Data AnalystRemote Clinical Research Coordinator
Primary RoleAnalyzes clinical trial data, manages databases, generates reportsCoordinates trial activities, manages site operations, ensures protocol compliance
Required SkillsData analysis, statistical software, attention to detailCommunication, organization, regulatory knowledge
Work EnvironmentRemote, primarily computer-basedRemote or onsite, site management
Common CertificationsCertified Clinical Data Manager (CCDM), related data certificationsCertified Clinical Research Professional (CCRP), site management certifications

The Remote Clinical Trials Data Analyst focuses on analyzing and managing clinical data remotely, while the Remote Clinical Research Coordinator handles trial coordination and site management. Both roles require understanding of clinical research but differ in daily tasks and skill sets.

More about Remote Clinical Trials Data Analyst jobs
What cities are hiring for Remote Clinical Trials Data Analyst jobs? Cities with the most Remote 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 Remote Clinical Trials Data Analyst jobs? States with the most job openings for Remote Clinical Trials Data Analyst jobs include:
What job categories do people searching Remote Clinical Trials Data Analyst jobs look for? The top searched job categories for Remote Clinical Trials Data Analyst jobs are:
Remote Clinical Trials Data Analyst jobs near you
Infographic showing various Remote Clinical Trials Data Analyst job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 64% Full Time, 30% Part Time, and 5% Contract. Highlights an 81% Physical, 8% Hybrid, and 11% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.
Senior Clinical Trials Scientist

Senior Clinical Trials Scientist

CG Oncology, Inc.

Remote

$150K - $170K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

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

Job description

About CG Oncology, Inc.
Are you ready to make a difference in the world and become part of our patient-centered team that is focused on Attacking Bladder Cancer for a Better Tomorrow? At CG Oncology, we believe that by having exceptionally talented individuals on our team who share our passion and enjoy working together, we can truly achieve our Vision and Mission to benefit patients around the world.
Every day we are making significant advancements across our multiple pipelines and are growing rapidly to meet the needs of our patients who cannot afford to wait to benefit from our novel immunotherapies. Please review this job posting and our Values and if they resonate with you and are what you expect from your organization and team, then we would like to hear from you.
About the role
The Senior Clinical Trials Scientist (Sr CTS) provides scientific leadership and mentorship across Clinical Development and Operations teams but does not include formal line management or direct reports. This individual will lead the scientific and strategic execution of global Phase II-III clinical trials, acting as a primary scientific expert in cross-functional teams and external collaborations. The Sr. CTS contributes to the development of clinical strategy and ensures the integrity of clinical trial design, implementation, data analysis, and reporting. The ideal candidate is a seasoned professional with demonstrated ability to lead clinical programs in complex therapeutic areas, particularly oncology.
Location: Remote
Essential Functions
  • Provide scientific leadership for the planning, design, and implementation of complex Phase II-III clinical trials, ensuring adherence to regulatory, ethical, and scientific standards.
  • Author and/or provide critical review of study protocols, amendments, informed consent documents, clinical study reports (CSRs), and other clinical documentation.
  • Serve as a scientific liaison across cross-functional teams including Clinical Operations, Regulatory Affairs, Pharmacovigilance, Biometrics, Quality, and Clinical Supply Chain to drive timely and efficient execution of studies.
  • Partner with external stakeholders (CROs, vendors, investigators) to ensure study conduct meets internal quality standards and regulatory compliance.
  • Oversee and provide scientific input into data review, including listings, tables, and figures, and contribute to interim and final data analysis and interpretation.
  • Participate in the development of regulatory documents, including briefing books, IND/NDA/BLA submissions, and responses to health authority inquiries.
  • Support and/or lead the preparation and conduct of investigator meetings, advisory boards, and scientific presentations.
  • Mentor and provide technical guidance to Clinical Trials Scientists and other junior team members through matrixed and collaborative relationships.
  • Contribute to clinical strategy discussions and development plans in collaboration with medical and strategic leadership.

Qualifications
  • Master's degree in a scientific or health-related field (e.g., biology, pharmacology, public health).
  • Seven plus (7+) years of experience in clinical research/drug development, with demonstrated experience in clinical trial design and execution.
  • Experience with regulatory document development and regulatory agency interactions
  • Strong knowledge of ICH-GCP guidelines, FDA/EMA regulations, and clinical trial methodology.
  • Exceptional written and verbal communication skills, including clinical writing and data interpretation.
  • Proven ability to manage multiple projects with high attention to detail in a fast-paced, high-growth environment.
  • Demonstrated scientific leadership and mentoring capabilities in cross-functional or matrixed environments.
  • Availability for ~10% domestic and international travel, including overnight stays.
  • Flexible work hours to accommodate global team collaboration

Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.
Total Rewards
CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our global team of high-performing employees focused on developing bladder-saving therapeutics for patients afflicted with bladder cancer.
  • HIGHLY COMPETITIVE SALARIES
  • ANNUAL PERFORMANCE/MERIT REVIEWS
  • ANNUAL PERFORMANCE BONUSES
  • EQUITY
  • SPECIAL RECOGNITION

Well-Being Benefits
In addition to our Total Rewards, CG Oncology offers a variety of Well-Being Benefits to meet the majority of the needs of our unique and growing workforce. These benefits are designed to support our team to achieve a healthy balance between work and their personal lives to remain refreshed, engaged, and creating an environment where each person can find a deeper meaning and purpose in their work.
Well-Being Benefits eligibility begins the 1st of the month after hire. While a majority of these benefits are for our US-based workforce, we continue to assess comparable levels of benefits for our international team members that are aligned with country-specific regulations and their national programs offered.
  • FULLY REMOTE WORK ENVIRONMENT
  • REST AND RECHARGE BENEFITS - Unlimited Flexible Time Off
  • HOLIDAYS -In 2026 we will observe 14 holidays
  • RETIREMENT - 401K with 100% company Safe Harbor match up to 4% of base salary
  • HEALTH (MEDICAL, DENTAL, VISION) - PPO & HDHP - Cigna/Principal
  • HEALTH SPENDING ACCOUNTS - HSA (with Annual Company Contribution), FSA, FSA-DC
  • ILLNESS & DISABILITY PROTECTION - Company Paid LTD Coverage + Voluntary Plans
  • LIFE INSURANCE - Company Paid 1 x base salary + Voluntary Plans
  • ADDITIONAL EXCLUSIVE BENEFITS - Voluntary Legal, Pet, Plus More

CG Oncology is an Equal Opportunity Employer:
All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. At CG Oncology, we are building a community of intelligent and passionate team members that share our Vision, Mission and Values, and while the biotechnology space can feel limited in BIPOC, non-binary and even female representation, we endeavor to make hiring decisions that will continue to grow and support our team in the direction of maintaining cultural diversity and sustainability.
The pay range for this role is:
150,000 - 170,000 USD per year (Remote)

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