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Trial Disclosure Transparency Jobs (NOW HIRING)

Manager, Clinical Pharmacology

Collegeville, PA ยท On-site

$106K - $176K/yr

Experience interpreting PK and PK/PD data and integrating this knowledge into the clinical trial ... If you are applying for the role in an secondary job posting location where pay transparency ...

Manager, Clinical Pharmacology

New York, NY ยท On-site

$106K - $176K/yr

Experience interpreting PK and PK/PD data and integrating this knowledge into the clinical trial ... If you are applying for the role in an secondary job posting location where pay transparency ...

Manager, Clinical Pharmacology

Bothell, WA ยท On-site

$106K - $176K/yr

Experience interpreting PK and PK/PD data and integrating this knowledge into the clinical trial ... If you are applying for the role in an secondary job posting location where pay transparency ...

Manager, Clinical Pharmacology

San Diego, CA ยท On-site

$106K - $176K/yr

Experience interpreting PK and PK/PD data and integrating this knowledge into the clinical trial ... If you are applying for the role in an secondary job posting location where pay transparency ...

Manager, Clinical Pharmacology

Groton, CT ยท On-site

$106K - $176K/yr

Experience interpreting PK and PK/PD data and integrating this knowledge into the clinical trial ... If you are applying for the role in an secondary job posting location where pay transparency ...

Prepare for hearings, mediation and trial Skills * Proven working experience as a litigation ... Pay Transparency Notice Pursuant to applicable law, this position includes a good-faith salary or ...

Prepare for hearings, mediation and trial Skills * Applicable knowledge of motions, discovery ... Pay Transparency Notice Pursuant to applicable law, this position includes a good-faith salary or ...

Director, Regulatory Affairs

New York, NY ยท On-site +1

$164K - $216K/yr

... trial applications, marketing authorization applications, orphan drug designation applications, pediatric submissions, etc.). Create, collaborate and comply with disclosure and transparency policies ...

Director, Regulatory Affairs

New York, NY ยท On-site

$164K - $216K/yr

... trial applications, marketing authorization applications, orphan drug designation applications, pediatric submissions, etc.). Create, collaborate and comply with disclosure and transparency policies ...

Manager, Clinical Data Research (Remote)

Irvine, CA ยท On-site +1

$116K - $193K/yr

... trial data. Leads the data management team, enforces regulatory compliance and ensures databases ... S. work location and transparency guide to find the pay range for your location. Travel Percentage ...

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Trial Disclosure Transparency information

See salary details

$50K

$120.8K

$192.5K

How much do trial disclosure transparency jobs pay per year?

As of Jul 23, 2026, the average yearly pay for trial disclosure transparency in the United States is $120,815.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $138,500.00 per year, depending on experience, location, and employer.

What is Trial Disclosure Transparency?

Trial Disclosure Transparency refers to the practice of publicly sharing information about clinical trials, including their design, methods, results, and potential outcomes. This transparency aims to ensure that data from clinical research is accessible to researchers, healthcare professionals, and the public to promote trust, accountability, and scientific progress. It often involves registering trials in public databases and publishing results, regardless of study outcomes. Regulatory agencies and organizations encourage or require such transparency to prevent selective reporting and to enhance patient safety.

What are the primary challenges faced in a Trial Disclosure Transparency role, and how can they be managed?

Professionals in Trial Disclosure Transparency roles often encounter challenges related to balancing regulatory compliance with the protection of confidential information. They must navigate evolving global requirements for clinical trial registration and results disclosure, ensuring accuracy and timeliness. Managing communications between clinical teams, legal departments, and regulatory authorities is essential, as is staying current with updates from agencies like the FDA and EMA. Developing strong project management and collaboration skills helps address these demands and ensures successful, compliant disclosures.

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

To thrive as a Trial Disclosure Transparency Specialist, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), ICH guidelines, and systems for tracking disclosure deadlines is essential, and certifications like CCRA or RAC are beneficial. Strong attention to detail, project management, and effective communication skills help ensure timely and accurate trial data reporting. These competencies are vital to maintaining compliance, supporting public trust, and ensuring transparency in clinical research.

What is the difference between Trial Disclosure Transparency vs Paralegal?

AspectTrial Disclosure TransparencyParalegal
Primary RoleProviding clear, accurate information about trial procedures and disclosures to clients and stakeholdersSupporting attorneys with legal research, document preparation, and case management
Required CredentialsLegal knowledge, understanding of trial procedures, communication skillsAssociate degree or paralegal certification, legal research skills
Work EnvironmentCourts, legal offices, or client meetingsLaw firms, corporate legal departments, government agencies

Trial Disclosure Transparency focuses on ensuring clear communication of trial disclosures, while paralegals assist attorneys with case preparation. Both roles require legal knowledge but differ in responsibilities and work settings.

More about Trial Disclosure Transparency jobs
What cities are hiring for Trial Disclosure Transparency jobs? Cities with the most Trial Disclosure Transparency job openings:
What states have the most Trial Disclosure Transparency jobs? States with the most job openings for Trial Disclosure Transparency jobs include:
Infographic showing various Trial Disclosure Transparency job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $120,815 per year, or $58.1 per hour.
Global Medical Communication Manager (Hybrid- Lawrenceville, NJ)

Global Medical Communication Manager (Hybrid- Lawrenceville, NJ)

Stage 4 Solutions Inc

Lawrenceville, NJ โ€ข On-site

Contractor

Medical, Retirement

Posted 17 days ago


Job description

Global Medical Communication Managerย (Hybrid โ€“ Lawrenceville, NJ)ย 

We are seeking a Global Medical Communication Manager for our global pharmaceutical client. The focus of the role is to lead across the client matrix to develop andย timelyย delivery of strategically aligned medical publications, scientific content, medical information, medical education, training content, and congress presentations.ย 

This is a 40-hour per-week,ย 6-month contract (extensions possible), 50% onsite at the clientโ€™s office in Lawrenceville, NJ.ย 

This is a W2 role as a Stage 4 Solutions employee. Health benefits and a 401K are offered.ย 

Responsibilities:ย ย 

The Medical Communications manager is accountable for the following:ย 

Medical Communications Strategy:ย 

  • Ensures endorsement of medical communications plans by relevant governance bodies prior to execution, and continuously develops and maintains plans in conjunction with scientific landscape and in alignment with Local Market Medical, Worldwide (WW) Medical and medical market-level strategyย 

  • Serves as the Medical Communications point of contact between WW/ and other matrix partnersย 

  • Provides medical communications management oversightย 

  • Enhances bi-directional communication by understanding and sharing the WW medical communications plans to Medical and raises needs to WW Medical/Medical Communications teams, ensuring country/global level of awareness & connectivity including vendor oversight.ย 

  • Understand the communication needs and own the pull-through and execution of the Scientific Narrative, development & execution of functionally integrated publication plan, content plan, and application to the Scientific Communication Platform (SCP).ย 

  • Must have strong business acumen, ability to interface with market matrix partners & manage Medical Communications budgetย 

Data Dissemination:ย 

  • Serve as a subject matter expert to internal audiences related to communication landscape, HCP preferences, publication and scientific content planning, data disclosure / dissemination, and represent scientific communications to external investigators, key authors and journal editors.ย 

  • Promotes and reinforces principles among authors and internal publication stakeholder community, ensuring publications are authored, written, and reviewed according to publication best practices and standards and policies ensuring publication & scientific content standards are aligned with Good Publication Practices and industry standards, and all employees engaged in publication activities follow Good Publication Practices guidance with the highest degree of integrity, quality and transparency.ย 

  • Demonstrates understanding of therapeutic disease areas, expertise to support the establishment of strong working collaborations with both internal and external disease-area experts to ensure quality data analysis, interpretation, communication planning & data disclosure/dissemination.ย 

  • Ensures collection of insights to deliver high quality medical communication that enables the most impactful dialogue and interactions with customers.ย 

  • Identifies and drives opportunities to enhance processes, tools, operating procedures, and outsourcing strategy to ensure consistent delivery and alignment of standardsย 

Stakeholder Engagement:ย 

  • Fostering collaborative relationships with academic & clinical experts, publishers, medical associations & other relevant key stakeholder groups; participating in external initiatives to foster trust and respect amongst academic and medical publishing communityย 

  • Partners with TA Medical Communication Leads, Market Medical and other stakeholder to assess, plan, and allocate resources (budget, medical writing, biostatistical services) to ensure timely delivery of high-quality medical communicationsย 

  • Partners externally with 3rd party vendors to ensure the appropriate balance of internal and external execution of workย 

  • Establishes clear metrics aligned & regularly communicates metrics with key medical stakeholdersย 

  • Other responsibilities:ย 

  • High performing, externally focused which emphasizes teamwork, cooperation, personal accountability, and a commitment to quality; models behaviors and reinforces such behaviors at all levels in the organizationย 

  • Ensure preparation for audit and inspection readinessย 

  • Ensuring diversity and inclusion in decision making, organization and talent developmen

Requirements:ย ย 

  • 3+ years of Pharmaceutical/Healthcare industry experience with a focus on medical communications; experience in both local country & global preferredย ย 

  • Experience leading medical communications across all phases of drug development and commercializationย ย 

  • Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate andย collaborate. Ability to analyze and interpret trial dataย 

  • Experience working cross-functional, with cross-cultural project teams, and collaborating across matrix, markets, and global geographiesย 

  • Ability to influence and negotiate appropriate solutions; ability to establish strong stakeholder relationshipsย 

  • Ability to flexibly schedule andย participateย in teleconferences and virtual meetings across different time zones. Ability to travel (domestically and internationally)ย 

  • Advance scientific degree, PharmD, PhD or MD preferredย 

Pleaseย submitย your resume to our network atย https://www.stage4solutions.com/careers/ย (please apply to theย Global Medical Communication Manager (Hybrid โ€“ Lawrenceville, NJ)ย role).ย 

Please feel free to forward this project opening to others who may be interested.ย 

Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidatesโ€™ qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.ย 

Compensation: $100/hr. - $102.96/hr.ย 

#LI-SW1ย ย ย