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Remote Clinical Trial Data Transparency Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

Fortrea

Clinical Trial Manager

Remote US or Canadian based. Job Overview: The Clinical Trial Manager has ownership in the clinical ... Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint ...

Ossium Health

Clinical Trial Manager

San Francisco, CA · On-site +1

$145K - $165K/yr

About the Job We are hiring a Clinical Trial Manager to support the successful execution of our ... as a remote work day * Ability to travel as needed (10% - 15%) * Qualified candidates must be ...

WEP Clinical

Clinical Trial Project Manager

... data integrity, and high-quality delivery in compliance with applicable regulations. This role ... LI-remote We may use artificial intelligence (AI) tools to support parts of the hiring process ...

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 ...

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 ...

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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 26, 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:
What states have the most Remote Clinical Trial Data Transparency jobs? States with the most job openings for Remote Clinical Trial Data Transparency jobs include:
What job categories do people searching Remote Clinical Trial Data Transparency jobs look for? The top searched job categories for Remote Clinical Trial Data Transparency jobs are:
Remote Clinical Trial Data Transparency jobs near you
Infographic showing various Remote Clinical Trial Data Transparency job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.
Oncology-CRA/Data Management, Analytics & Statistical Support

Oncology-CRA/Data Management, Analytics & Statistical Support

BriaCell Therapeutics Corp.

Newark, NJ • Remote

$80K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 27 days ago

Job description

Hybrid/Remote – Travel Required
We are seeking a flexible and experienced Oncology Clinical Research Coordinator (CRC) or a newly transitioned Clinical Research Associate (CRA) to join our dynamic Clinical Operations team. This hybrid role supports oncology clinical trials and is open to candidates with experience in CROs or academic institutions, even if they lack direct sponsor experience.
In addition to clinical operations expertise, the ideal candidate will bring a strong background in data management, data analytics, and statistical interpretation, with demonstrated experience analyzing clinical trial data to support study execution, monitoring, and decision‐making.
We also welcome international clinical research professionals who are authorized to work in the United States for any employer and bring prior hands‐on experience with U.S.-based clinical research trials and data management.
Remote work flexibility is available, with the expectation that team members adhere to each site's operational policies and requirements. Strong communication skills are essential, with an emphasis on real‐time responsiveness to logistical and operational questions from sites.

Key Responsibilities
Site Monitoring

  • Conduct regular on‐site and remote monitoring visits to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements
  • Execute monitoring plans tailored to each study
  • Review case report forms (CRFs), source documentation, and data entries for accuracy, completeness, and consistency
  • Identify data discrepancies and collaborate with Data Management to ensure timely query resolution
  • Resolve site-related issues and manage investigational product logistics
  • Maintain strong relationships with site staff and provide real-time support on eligibility, protocol logistics, and operational questions
  • Deliver high-quality presentations during SQVs/SIVs


Data Management, Analytics & Statistical Support

  • Review and interpret clinical trial data to identify trends, risks, and data quality issues
  • Support data cleaning, query management, and reconciliation activities in collaboration with Data Management teams
  • Analyze enrollment trends, protocol deviations, and site performance metrics
  • Apply basic statistical concepts to interpret trial data and support operational decision-making
  • Contribute to development of data tracking tools, dashboards, and performance reports
  • Ensure accuracy and completeness of data within EDC and other clinical systems (CTMS, IRT)
  • Participate in cross-functional data review meetings and support data-driven study execution


Recruitment and Retention Strategies

  • Develop and implement tailored patient recruitment and retention plans using approved vendors
  • Analyze recruitment data and site performance metrics to drive strategic improvements
  • Collaborate with site staff to identify and overcome recruitment barriers
  • Track and report recruitment KPIs and provide actionable insights to the project team
  • Prioritize recruitment support and re-training for underperforming sites
  • Conduct in‐service training and apply engagement strategies to improve enrollment


Communication and Collaboration

  • Serve as the primary point of contact for study sites
  • Collaborate cross-functionally with Clinical Operations, Data Management, Biostatistics, and Regulatory teams
  • Prepare and present study progress reports, including data trends and analytics insights, to stakeholders


Training and Development

  • Train and mentor site staff on protocols, GCP, data entry expectations, and system use (EDC/CTMS)
  • Stay current with industry trends, data management practices, and evolving regulatory expectations


Qualifications

  1. Bachelor’s degree in life sciences, nursing, or related field required
  2. Clinical degree (MD, RN, PharmD, or equivalent).
  3. Experience in data management, clinical data review, and/or data analytics required
  4. Background in statistics, epidemiology, or data analysis strongly preferred
  5. Minimum 2–3 years of oncology clinical research experience (CRC or CRA)
  6. Experience in CROs or academic institutions acceptable in lieu of direct sponsor experience
  7. Strong understanding of GCP, ICH guidelines, and regulatory requirements
  8. Demonstrated ability to interpret clinical trial data and apply analytical thinking
  9. Proficiency with EDC systems, CTMS, and data tracking/reporting tools
  10. Excellent communication, presentation, and problem-solving skills
  11. Ability to respond promptly to site inquiries and logistical needs
  12. Willingness to travel regularly based on monitoring and recruitment requirements

Company Description

BriaCell Therapeutics is a clinical-stage immuno-oncology company developing novel cell-based immunotherapies for solid tumors, including metastatic breast cancer. Our mission is to advance innovative immunotherapy approaches that improve outcomes for patients with difficult-to-treat malignancies.