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Remote Clinical Trial Data Transparency Jobs (NOW HIRING)

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 ...

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 ...

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 ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

University of Utah

Clinical Data Managers

Salt Lake City, UT · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

University of Utah

Clinical Data Managers

Campus, IL · On-site +1

$50K - $69K/yr

This position offers a flexible, mostly remote work schedule for candidates who reside in the state ... Compile, analyze, clean, and validate clinical trial data. Identify and resolve discrepancies and ...

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All JobsRemote Clinical Trial Data Transparency Jobs

Remote Clinical Trial Data Transparency information

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

As of Jun 9, 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.

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What cities are hiring for Remote Clinical Trial Data Transparency jobs? Cities with the most Remote Clinical Trial Data Transparency job openings:
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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 May 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 75% Physical, 5% Hybrid, and 20% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.
Clinical Trial Manager/Senior Clinical Trial Manager

Clinical Trial Manager/Senior Clinical Trial Manager

Lexeo Therapeutics

New York, NY • On-site, Remote

$143K - $180K/yr

Full-time

Posted 20 days ago

Job description

Role Summary
The Clinical Trial Manager (CTM) or Senior Clinical Trial Manager (Sr. CTM) leads the execution of global clinical studies from startup through close-out. The CTM/Sr. CTM partners closely with cross-functional teams and external vendors to deliver high-quality clinical trials on time and within budget while ensuring compliance with regulatory standards. The CTM will independently manage study execution, while the Sr. CTM will lead more complex programs with broader strategic and cross-functional responsibilities.
Primary Responsibilities
Clinical Trial Execution
  • Lead day-to-day management of clinical studies to ensure delivery against timelines, budget, and quality expectations
  • Drive study milestones and proactively identify and mitigate risks

Vendor & CRO Management
  • Oversee CROs, laboratories, and vendors to ensure performance aligns with scope, timelines, and budget
  • Manage vendor relationships, including scope changes, issue resolution, and ongoing performance oversight

Cross-Functional Collaboration
  • Partner with internal stakeholders across Clinical, Regulatory, Data Management, and other functions
  • Serve as a central operational lead to ensure alignment and efficient study execution

Study Planning & Strategy
  • Contribute to study planning, including timelines, resource plans, budgets, and risk management strategies
  • Provide operational input into protocol development, feasibility, and study design

Site & Study Oversight
  • Act as the primary sponsor contact for study sites
  • Oversee site startup and ongoing site management activities
  • Ensure proper sample handling, data flow, and protocol adherence

Quality & Compliance
  • Ensure compliance with ICH/GCP, FDA regulations, and company SOPs
  • Maintain inspection readiness and support audits and regulatory inspections
  • Ensure completeness and integrity of the Trial Master File (TMF)

Documentation & Communication
  • Author and review study plans, operational documents, and training materials
  • Communicate study status, risks, and mitigation plans to stakeholders

Continuous Improvement
  • Contribute to process improvements and operational excellence initiatives
  • (Sr. CTM) Lead cross-study or departmental initiatives

Required Skills and Qualifications
  • Bachelor's degree in life sciences or a related field; advanced degree preferred
  • Clinical Trial Manager: minimum 7 years of clinical research experience; 4 years with advanced degree
  • Senior Clinical Trial Manager: experience leading complex or global studies, worked on a clinical study from concept to database lock
  • Strong knowledge of ICH/GCP, FDA regulations, and clinical trial operations
  • Experience managing CROs and other external vendors
  • Proven ability to manage timelines, budgets, and multiple priorities
  • Excellent communication, problem-solving, and leadership skills
  • Demonstrated leadership skills
  • Ability to work effectively in a fast-paced, collaborative environment
  • Ability to travel to sites as needed, including international travel
  • Ability to work Eastern Time Zone and travel to New York HQ quarterly

$143,350 - $180,000 a year
Compensation is dependent on qualifications and experience
About Lexeo
Lexeo Therapeutics is a clinical-stage genetic medicine company headquartered in New York City, pioneering cardiac genetic medicine candidates to treat the root causes of inherited cardiovascular diseases. Our lead program, LX2006, targets cardiomyopathy associated with Friedreich's Ataxia and anchors a broader pipeline addressing genetically defined conditions such as hypertrophic and arrhythmogenic cardiomyopathies. Backed by a strong financial foundation, Lexeo is positioned to translate groundbreaking science into durable clinical impact.
Our work culture is a hybrid model with 2 days/week in the New York City office and 3 days working from home.
Lexeo Therapeutics is an EEO employer committed to an exciting, diverse, and enriching work environment.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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