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Vice President Clinical Trial Data Transparency Jobs

Codera

Vice President, Clinical Development

San Diego, CA · Remote

$345K - $375K/yr

... clinical trial lifecycle, including safety monitoring, data interpretation and risk management ... Collaborate with the Vice President, Regulatory Affairs in the development and execution of ...

Absci Corporation

VP, Clinical Development

$355K - $415K/yr

The Vice President, Clinical Development serves as a senior leader within Clinical Development, accountable for clinical trial design, execution, regulatory strategy, data integrity, and cross ...

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

As of Aug 13, 2026, the average hourly pay for vice president clinical trial data transparency in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.

What is the difference between Vice President Clinical Trial Data Transparency vs Director Clinical Trial Data Transparency?

AspectVice President Clinical Trial Data TransparencyDirector Clinical Trial Data Transparency
ResponsibilitiesStrategic oversight, policy development, executive leadershipOperational management, project coordination, team supervision
Required CredentialsAdvanced degree (PhD, MD, or equivalent), extensive industry experienceBachelor's or master's degree, relevant industry experience
Work EnvironmentExecutive offices, cross-functional leadership teamsDepartmental teams, project-focused settings
Industry UsageCommonly used in large pharma and biotech companiesUsed across various biotech and pharmaceutical organizations

The Vice President Clinical Trial Data Transparency typically holds a senior leadership role with strategic responsibilities, while the Director focuses on managing daily operations and project execution. Both roles require industry-specific knowledge, but the VP position involves broader oversight and policy development.

What cities are hiring for Vice President Clinical Trial Data Transparency jobs? Cities with the most Vice President 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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Vice President Clinical Trial Data Transparency jobs near you

Vice President, Clinical Development Operations

Tempus

Remote

Full-time

Posted 29 days ago

Job description

Passionate about precision medicine and advancing the healthcare industry?
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.
The Vice President, Clinical Development Operations provides strategic leadership and operational oversight for the execution of clinical studies dedicated to evidence generation across the Tempus portfolio. This role is primarily responsible for ensuring that all evidence-generating clinical development studies are conducted with the highest standards of quality, on time, within budget, and in full compliance with global regulatory requirements. The VP will focus on driving operational excellence to deliver robust clinical data that supports product validation, regulatory submissions, and clinical evidence goals.
Key Responsibilities
Strategic & Clinical Trial Leadership
  • Overall Study Conduct: Hold primary accountability for the operational planning, management, and execution of clinical trials designed for clinical evidence generation.
  • Metric-Driven Performance: Drive performance against key trial metrics, including site activation, patient enrollment, data quality, budget adherence, and alignment with corporate goals and regulatory requirements.
  • Operational Excellence: Develop and implement optimized operational strategies to enhance trial efficiency, reduce complexity, and accelerate data delivery timelines.
  • Resource & Budget Management: Actively participate in budget planning, financial forecasting, and resource allocation for the evidence generation operations unit to ensure optimal performance.
Clinical Data Integration & Workflow Management
  • Data Integrity & Flow: Collaborate closely with Biostatistics and Data Management teams to ensure the timely, accurate, and high-quality flow of trial data into the clinical database, facilitating efficient data cleaning, analysis, and database lock.
  • Cross-Functional Collaboration: Interact closely and establish seamless workflows with cross-functional leaders to ensure that clinical trial data from all sources is accurately captured and reconciled.

Cross-Functional Leadership & Team Management
  • Team Leadership: Lead, mentor, and develop a high-performing operations team capable of managing a focused portfolio of clinical evidence generation studies.
  • Stakeholder Alignment: Serve as the primary operational leader for evidence generation trial conduct, ensuring tight alignment and communication with Clinical Development, Regulatory Affairs, Project Management, and other key stakeholders.

Quality & Regulatory Compliance
  • GCP Compliance: Ensure all evidence-generation trial activities are conducted in strict accordance with Good Clinical Practice (GCP), ICH guidelines, and global regulatory standards.
  • Inspection Readiness: Maintain a constant state of inspection readiness for all evidence-generation clinical trials and support senior leadership during regulatory authority inspections (e.g., FDA).

Requirements
  • Bachelor's degree in a scientific, life sciences, or healthcare discipline required; advanced degree (MS, PhD, PharmD) preferred.
  • 13+ years of progressive clinical trial operations experience within pharma, biotech, or medical device sectors, with a distinct focus on managing trials for clinical evidence generation.
  • 5+ years managing and building high-performing clinical operations teams.
  • Deep, demonstrable knowledge of GCP, ICH guidelines, and experience defending clinical data/sites during regulatory authority inspections (e.g., FDA).
  • Proven track record of partnering successfully with Biostatistics, Data Management, and Medical Directors to achieve timely database locks.

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We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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