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Contract Clinical Trial Data Transparency Jobs (NOW HIRING)

Biogen

Senior Clinical Trial Transparency Specialist

$116K - $155K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This position reports to the Head, Clinical Trial Transparency Operations and works closely with Clinical Development, Regulatory Affairs, Medical Writing, Data Management, and external service ...

New

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and ... other contract personnel. * Manage study timelines and metrics to ensure completion of study ...

Cytokinetics

Contract Clinical Systems Specialist

$75 - $86/hr

The Contract Clinical Systems Specialist is responsible for supporting the lifecycle management of ... Understanding of clinical trial data and regulations (CDISC, Good Clinical Practice, 21 CFR Part 11)

Parexel

Clinical Trial Leader

Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring) * Verifies and ... Makes effective use of resources, and proactively strives for transparency and clarity to ...

Ipsen

Clinical Trial Administrator

Cambridge, MA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Ensure the information is properly recorded in the Data Transparency system (COLLECT), implement ... Generate contract templates within the Ipsen dedicated system (ARIBA), follow-up until the clinical ...

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manage and lead all aspects of clinical trial data management activities from study start-up to database lock. * Develop and implement data management plans, data validation plans, edit check plans ...

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Contract Clinical Trial Data Transparency information

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

As of Aug 19, 2026, the average hourly pay for contract clinical trial data transparency in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is a contract clinical trial data transparency professional?

A Contract Clinical Trial Data Transparency professional is responsible for ensuring that data from clinical trials are disclosed and reported in accordance with legal, regulatory, and industry standards. They typically work on a contractual basis, helping pharmaceutical or biotech companies comply with data transparency requirements such as posting results on public registries, redacting sensitive information, and supporting data-sharing initiatives. Their work helps promote scientific integrity, protect patient privacy, and maintain public trust in clinical research.

What are some common challenges faced in a contract clinical trial data transparency role, and how are they typically addressed?

Professionals in Contract Clinical Trial Data Transparency often encounter challenges such as navigating complex global regulations, ensuring timely anonymization of sensitive data, and balancing transparency with patient privacy. These challenges are typically addressed by closely collaborating with legal, data management, and clinical teams, as well as staying up-to-date on evolving guidelines from regulatory authorities. Utilizing robust data anonymization tools and standardized processes also helps maintain compliance while meeting transparency requirements.

What are the key skills and qualifications needed to thrive as a contract clinical trial data transparency specialist, and why are they important?

To thrive in Contract Clinical Trial Data Transparency, you need a solid understanding of clinical research processes, regulatory requirements (such as GDPR and FDA guidelines), and strong data management skills, often supported by a degree in life sciences or a related field. Familiarity with data anonymization tools, clinical trial management systems (CTMS), and regulatory submission platforms is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are vital soft skills for managing complex documentation and collaborating across teams. These skills ensure the accurate, compliant, and timely disclosure of clinical trial data, supporting transparency and public trust in research.

What is the difference between Contract Clinical Trial Data Transparency vs Clinical Data Manager?

AspectContract Clinical Trial Data TransparencyClinical Data Manager
Primary FocusEnsuring transparency and accessibility of clinical trial data to stakeholders and the publicManaging and validating clinical trial data for accuracy and completeness
Work EnvironmentContract-based, often project-specific, with collaboration across sponsors, regulators, and CROsIn-house or CRO setting, focused on data collection, cleaning, and database management
Required CredentialsKnowledge of clinical trial regulations, data sharing policies, and industry standardsDegree in life sciences, biostatistics, or related field; experience with clinical data systems

Contract Clinical Trial Data Transparency professionals focus on making clinical data accessible and compliant with transparency regulations, while Clinical Data Managers handle the collection, validation, and management of clinical trial data to ensure quality and integrity. Both roles are essential in the clinical research process but differ in their primary objectives and daily tasks.

What cities are hiring for Contract Clinical Trial Data Transparency jobs?

Cities with the most Contract 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 Contract Clinical Trial Data Transparency jobs?

States with the most job openings for Contract Clinical Trial Data Transparency jobs include:

Contract Clinical Trial Data Transparency jobs near you
Infographic showing various Contract Clinical Trial Data Transparency job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager (contract)

ALX Oncology Inc.

South San Francisco, CA • On-site

$70/hr

Contractor

Posted 2 days ago

New

Job description

Reporting to the Executive Director, Clinical Operations, the contract Clinical Trial Manager (CTM) will manage the day-to-day operational execution of global clinical trials from study start-up through closeout. The contract CTM will be responsible for coordinating study activities, managing timelines and vendors, monitoring study and site performance, and working across functions to ensure study milestones and deliverables are achieved on time and to a high standard of quality.
This is a 6- to 12-month contract assignment offering approximately 40 hours per week. The anticipated pay rate is approximately $70 per hour for candidates in the San Francisco Bay Area. Candidates who can work onsite in South San Francisco on Mondays and Tuesdays as part of the company's hybrid work model will be given preference. ADC clinical trial experience strongly preferred.
Qualified contractors should have experience that includes:
  • Managing day-to-day global clinical trial activities from study start-up through conduct and closeout, including timelines, milestones, enrollment, and study performance.
  • Supporting protocol review, feasibility assessments, site selection and activation, and protocol amendment activities.
  • Managing CROs, sites, and clinical vendors, including oversight of plans, deliverables, timelines, budgets, and quality.
  • Overseeing monitoring activities, including monitoring report review, U.S. co-monitoring, site performance, protocol deviations, data queries, and follow-up of significant issues.
  • Identifying operational risks and working cross-functionally to develop and implement mitigation strategies.
  • Leading study team meetings and communicating study progress, risks, decisions, and action items to internal and external stakeholders.
  • Ensuring study conduct and TMF quality are consistent with study protocols, ICH/GCP, applicable regulatory requirements, and inspection-readiness expectations.
  • Clinical operations experience in biotechnology, pharmaceutical, or CRO environments; ADC clinical trial experience strongly preferred.
  • Strong project management, communication, problem-solving, and organizational skills; proficiency with EDC, IRT, CTMS, and eTMF.
  • Ability to work effectively in a small, fast-paced biotech environment.

About ALX Oncology
ALX Oncology (Nasdaq: ALXO) is a clinical-stage biotechnology company advancing a pipeline of novel therapies designed to treat cancer and extend patients' lives. ALX Oncology's lead therapeutic candidate, evorpacept, has demonstrated potential to serve as a cornerstone therapy upon which the future of immuno-oncology can be built. Evorpacept is currently being evaluated across multiple ongoing clinical trials in a wide range of cancer indications. ALX Oncology's second pipeline candidate, ALX2004, is a novel EGFR-targeted antibody-drug conjugate with a differentiated mechanism of action. A Phase 1, dose-escalation trial of ALX2004 is ongoing in patients with EGFR-expressing solid tumors. More information is available at www.alxoncology.com and on LinkedIn @ALX Oncology.

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