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Clinical Trial Transparency Manager Jobs (NOW HIRING)

Ipsen

Clinical Trial Administrator

Cambridge, MA

Clinical Trial Administrator Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid ... When needed, liaise with the Local Transparency Manager (LTM) or the Global Transparency Manager.

Syneoshealth

OR · On-site

$80K - $145K/yr

Sr Medical Writer, Redaction (Clinical Trial Transparency) Syneos Health is a leading fully ... line management; technical and therapeutic area training; peer recognition and total rewards ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA

$115K - $200K/yr

We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and ... Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ...

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 ... Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ

$95K - $115K/yr

Clinical Trial Manager Marlton, NJ Hope is Here! Impulse Dynamics (USA), Inc. is a fast-growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac ...

Viking Therapeutics

Clinical Trial Manager

San Diego, CA · On-site

$110K - $140K/yr

The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...

VIKING THERAPEUTICS INC

Clinical Trial Manager

San Diego, CA · On-site

$110K - $140K/yr

The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...

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Civia Health

Clinical Trial Manager

... transparency, and performance accountability. Within this model, the Clinical Trial Manager (CTM ... is the country-level owner of study delivery outcomes and the primary advocate for the client ...

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Clinical Trial Transparency Manager information

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How much do clinical trial transparency manager jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for clinical trial transparency manager 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 the difference between Clinical Trial Transparency Manager vs Clinical Data Coordinator?

AspectClinical Trial Transparency ManagerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences, healthcare, or related field; certifications in clinical research or transparency are commonUsually holds a degree in health sciences, nursing, or related field; certifications in clinical data management may be preferred
Work EnvironmentWorks in regulatory, compliance, or clinical research departments, often within pharmaceutical or biotech companiesWorks in clinical trial data management, often within research organizations or clinical sites
Employer & IndustryPharmaceutical, biotech, or healthcare companies focusing on trial transparency and regulatory complianceResearch organizations, clinical trial sites, or CROs managing clinical data

The Clinical Trial Transparency Manager focuses on ensuring transparency and compliance of clinical trial data with regulatory standards, while the Clinical Data Coordinator manages the collection, validation, and organization of clinical trial data. Both roles require knowledge of clinical research processes but differ in their primary responsibilities and work settings.

What does a Clinical Trial Transparency Manager do?

A Clinical Trial Transparency Manager is responsible for ensuring that information about clinical trials is publicly available and compliant with global regulations. They oversee the registration of trials, disclosure of results, and publication of relevant data on public platforms like ClinicalTrials.gov and EudraCT. Their role also involves collaborating with cross-functional teams to maintain data accuracy and transparency, managing timelines for disclosure, and staying updated with changing regulatory requirements. Ultimately, they help promote trust and accountability in clinical research.

How does a Clinical Trial Transparency Manager typically collaborate with cross-functional teams to ensure compliance with disclosure requirements?

A Clinical Trial Transparency Manager works closely with regulatory affairs, data management, clinical operations, and legal teams to ensure all trial data and documentation meet global disclosure requirements. This collaboration often involves coordinating timelines, reviewing study results for public registries, and addressing queries from internal and external stakeholders. By facilitating clear communication across departments, the manager helps maintain data integrity and ensures that transparency standards are met efficiently. Regular meetings and shared project management tools are commonly used to streamline this cross-functional collaboration.

What are the key skills and qualifications needed to thrive as a Clinical Trial Transparency Manager, and why are they important?

To thrive as a Clinical Trial Transparency Manager, you need expertise in clinical research regulations, data disclosure requirements, and a solid understanding of Good Clinical Practice (GCP), often backed by a relevant life sciences degree. Familiarity with clinical trial registries, submission portals, and systems like EudraCT, ClinicalTrials.gov, and data anonymization tools is crucial. Attention to detail, strong project management, and excellent communication skills help ensure compliance and effective collaboration with cross-functional teams. These competencies are vital to ensure regulatory compliance, protect patient privacy, and uphold the integrity and public trust in clinical research.
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Clinical Trial Transparency Manager jobs near you
Infographic showing various Clinical Trial Transparency Manager job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 95% Full Time, 2% Part Time, 1% Temporary, and 1% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.
Sr. Clinical Trials Transparency & Disclosure Specialist

Sr. Clinical Trials Transparency & Disclosure Specialist

Celldex Therapeutics

New Haven, CT • On-site

$87K - $114K/yr

Other

Medical, Retirement, PTO

Posted 11 days ago

Job description

Overview
The Sr. Clinical Trials Transparency & Disclosure Specialist is responsible for supporting and executing Celldex Therapeutics' global clinical trial transparency and disclosure activities. This role ensures compliance with applicable regulatory requirements and company policies related to clinical trial registration, results disclosure, and public dissemination of clinical trial information.
Working collaboratively with Clinical Operations, Regulatory Affairs, Biostatistics, Medical Writing, Legal, and other cross-functional stakeholders, the Clinical Trials Transparency & Disclosure Specialist serves as a subject matter expert for transparency and disclosure requirements across the development portfolio. The role is accountable for the timely and accurate registration of clinical studies, submission of clinical trial results, maintenance of disclosure records, oversight of transparency-related processes, and continuous improvement of compliance practices. This position supports Celldex's commitment to regulatory compliance, scientific integrity, and public trust.
Responsibilities
  • Manage the planning, execution, and oversight of global clinical trial registration and results disclosure activities in accordance with applicable regulations and company policies.
  • Ensure timely and accurate registration, maintenance, and updating of clinical trial records in public registries, including ClinicalTrials.gov, CTIS, and other applicable regional registries.
  • Coordinate the preparation, review, and submission of clinical trial results disclosures in accordance with applicable regulations and company timelines.
  • Monitor evolving global disclosure regulations and industry guidance, assessing impact on company processes and compliance requirements.
  • Maintain complete and inspection-ready disclosure documentation, records, and compliance metrics.
  • Partner with cross-functional teams to gather required information and ensure accurate and consistent public reporting of clinical trial information.
  • Provide strategic guidance and operational support for transparency and disclosure activities throughout the clinical development lifecycle.
  • Support audits, inspections, and internal compliance reviews related to clinical trial transparency obligations.
  • Develop, implement, and continuously improve standard operating procedures (SOPs), work instructions, and training materials related to transparency and disclosure.
  • Track disclosure deadlines, identify compliance risks, and proactively implement mitigation strategies.
  • Generate reports and metrics to communicate program status, compliance performance, and key disclosure milestones to management.
  • Serve as a subject matter expert and resource for transparency and disclosure requirements across the organization.

Qualifications
  • Bachelor's degree in Life Sciences, Public Health, Regulatory Affairs, Clinical Research, or a related discipline; or an equivalent combination of education, training, and relevant professional experience.
  • 3-5 years of experience in clinical research, clinical operations, regulatory affairs, clinical disclosure, or a related pharmaceutical/biotechnology function.
  • Experience working with ClinicalTrials.gov, CTIS, EudraCT, or similar clinical trial registries preferred.
  • Familiarity with global clinical trial disclosure requirements, including FDAAA, EU Clinical Trial Regulation (CTR), and other applicable transparency requirements.
  • Experience working in a GCP-regulated environment.
  • Understanding of clinical trial processes and clinical development.
  • Knowledge of clinical trial transparency and disclosure requirements.
  • Excellent attention to detail and commitment to accuracy.
  • Strong written and verbal communication skills.
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Proficiency with Microsoft Office applications and clinical systems.
  • Accountability and ownership of assigned deliverables.
  • Proactive and solutions-oriented approach.
  • Commitment to compliance, quality, and continuous improvement.
  • Ability to build collaborative relationships across departments and with external partners.
  • High level of professionalism, integrity, and attention to detail.

Compensation
The expected base salary range for this position is $87,831 to $114,066
We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.

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