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Remote Clinical Trial Data Transparency Jobs (NOW HIRING)

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Lead cross-functional meetings with the Clinical Development, Clinical Operations, Data Management ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

4D Molecular Therapeutics

Clinical Trial Manager

The Clinical Trial Manager will support the Company's clinical trial activities. This position ... Perform and manage IP data review process on an ongoing basis * Perform site visits including site ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

... and data integrity. Responsibilities: * Provide operational leadership for one or more clinical ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

... and data integrity. Responsibilities: * Provide operational leadership for one or more clinical ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

ICON

Clinical Trial Associate

Blue Bell, PA · On-site +1

$32 - $43.75/hr

Tracking site performance metrics, analyzing data, and providing reports to enhance site management ... clinical trial management. Your Profile: You will bring relevant clinical research experience ...

ICON

Clinical Trial Manager II

Blue Bell, PA · On-site +1

Clinical Trial Manager - early oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...

ICON

Clinical Trial Manager

Blue Bell, PA · On-site +1

Participate in data review and discrepancy resolution. * Participate in coordinating efforts with ... Minimum of 5 years of clinical trial management experience in the biopharmaceutical industry or ...

UAB

CLINICAL RESEARCH REGULATORY COORDINATOR III

Tampa, FL · Remote

$55K - $89K/yr

... of trial data. This position completes regular site monitoring visits and any necessary audits ... This position is fully remote General Responsibilities * To prepare and submit multiple levels of ...

Icon plc

Clinical Trial Liaison

Lenexa, KS · Remote

Clinical Trial Liaison- US- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Icon plc

Clinical Trial Liaison

Lawrence, KS · Remote

Clinical Trial Liaison- US- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

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Remote Clinical Trial Data Transparency information

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How much do remote clinical trial data transparency jobs pay per hour?

As of Jul 5, 2026, the average hourly pay for remote clinical trial data transparency 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 is the difference between Remote Clinical Trial Data Transparency vs Remote Clinical Data Manager?

AspectRemote Clinical Trial Data TransparencyRemote Clinical Data Manager
Primary FocusEnsuring transparency and accessibility of clinical trial data to stakeholders and the publicManaging and maintaining clinical trial data for accuracy, integrity, and compliance
Required SkillsKnowledge of data sharing policies, regulatory requirements, and data privacyData management, database systems, and statistical software proficiency
Work EnvironmentTypically involves collaboration with regulatory bodies, sponsors, and data sharing platformsPrimarily works with clinical data, databases, and statistical teams
CertificationsOften requires knowledge of GCP, data privacy, and regulatory standardsCertifications like CDMP or SAS are common

In summary, Remote Clinical Trial Data Transparency focuses on making clinical data accessible and compliant with transparency policies, while Remote Clinical Data Managers handle the collection, validation, and management of clinical trial data to ensure quality and regulatory adherence.

More about Remote Clinical Trial Data Transparency jobs
What cities are hiring for Remote Clinical Trial Data Transparency jobs? Cities with the most Remote Clinical Trial Data Transparency job openings:
What are the most commonly searched types of Clinical Trial Data Transparency jobs? The most popular types of Clinical Trial Data Transparency jobs are:
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Remote Clinical Trial Data Transparency jobs near you
Infographic showing various Remote Clinical Trial Data Transparency job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 9% As Needed, 11% Full Time, 70% Part Time, 2% Temporary, and 7% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

FSP Principal Statistical Programmer (Remote)

Everest Clinical Research

Bridgewater, NJ • On-site, Remote

$112K - $175K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 19 days ago

Job description

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham Ontario, Canada with additional locations in: Bridgewater, New Jersey; Shanghai, China; Taipei, Taiwan; and multiple offices in Europe.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us...that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as FSP Principal Statistical Programmer for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities:
  1. Lead projects with higher level of complexity/challenges/difficulties. Lead efforts to resolve complex statistical programming issues or problems.
  2. Perform a leadership role in statistical programming projects by coordinating study team(s), overseeing timelines, assigning and following up on programming tasks, interacting with clients, and ensuring quality of programming deliverables.
  3. Assist statistical programming management in properly planning and allocating resources based on timelines, statistical programmers' skills and expertise, as well as availability.
  4. Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regulatory requirements.
  5. Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I - IV clinical trials, integrated clinical summaries, responses to requests from regulatory agencies, publication support, data explorations, data monitoring committee meetings, etc.
  6. Create SDTM mapping specifications and ADaM data specifications. Perform quality control (QC) review of these documents prepared by others.
  7. Create SDTM and ADaM define.xml files. Perform QC review of these files prepared by others.
  8. Perform 3rd level QC review on programming deliverables before their release to the clients.
  9. Perform QC review/assessment on regulatory submission programming documents, datasets, tables/listings/graphs (TLGs), and computer programs, etc.
  10. May lead programming efforts for drug development programs or for assigned client clusters.
  11. Provide training, mentorship, and technical guidance to less experienced Statistical Programmers or Biostatisticians who perform statistical programming.
  12. Monitor the compliance and adherence to the established data and programming standards, and statistical programming governing documents.
  13. May represent the company in interactions with clinical trial sponsors with regard to statistical programming projects and relevant businesses.
  14. Participate in the development of statistical programming policies, SOPs, guidelines, and good working practices.
  15. Participate in statistical programming project bidding or bid defense meetings.
  16. Work with document management specialists/archivists to plan and perform archival of the statistical programming datasets, outputs, documents, and final programs upon the completion of the assigned projects. Perform transfer of the archived files to the clinical trial sponsors.

Qualifications and Experience:
  1. M.Sc., M.A. or higher degree in Statistics, Biostatistics, Computer Science, or relevant fields.
  2. 10 (M.Sc., M.A.)/9 (Ph.D.) years' related experience.
  3. An in-depth knowledge of clinical trial data processing and manipulation, hands on statistical programming and analysis, requirements for assembling and presenting trial results to regulatory agencies. Knowledge of industry standards on how clinical trial data are structured, stored, analyzed, and presented. Knowledge of clinical trial regulatory and ICH requirements.
  4. Must demonstrate ability to effectively plan, control, and carry on tasks in SAS programming, statistical analysis, and submission of trial data and results to regulatory agencies. Must possess in-depth level understanding of the concept of standardization in data, programming, and statistical reporting of trial results, and its implication to the relevant functions and operations. Must have sound technical judgment and experience in process design and implementation in relevant areas. Strong leadership and drive to achieve goals will be required.

Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement / pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $112,000 - $175,000
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.ecrscorp.com
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#INDHP
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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