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Clinical Trial Data Transparency Jobs (NOW HIRING)

4D Molecular Therapeutics

Clinical Trial Manager

The Clinical Trial Manager will support the Company's clinical trial activities. This position ... Perform and manage data review process on an ongoing basis * Perform site visits including site ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness * Review, file, and track clinical trial documentation in accordance with SOPs and ...

Career Soft Solutions Inc

Lead Consultant

Groton, CT · On-site

Exposure to clinical trial data domains and standards Nice to have skills Solid understanding of Clinical trial data elements and metadata structures and Case Report Forms (CRFs) design, data capture ...

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy and timeliness * Review, file, and track clinical trial documentation in accordance with SOPs and ...

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

As of Jun 11, 2026, the average hourly pay for 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 a Clinical Trial Data Transparency job?

A Clinical Trial Data Transparency job involves managing the disclosure and sharing of clinical trial data in compliance with regulatory requirements and ethical guidelines. Professionals in this role ensure that trial data is accessible to researchers, healthcare professionals, and the public while protecting patient privacy and proprietary information. Responsibilities may include preparing clinical study reports, redacting sensitive data, and maintaining compliance with global transparency regulations. This role is critical for maintaining trust in clinical research and supporting scientific advancements.

What are the key skills and qualifications needed to thrive in the Clinical Trial Data Transparency position, and why are they important?

To thrive in Clinical Trial Data Transparency, you need a strong background in clinical research, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with data anonymization tools, CTIS (Clinical Trial Information System), CDISC standards, and regulations such as EMA Policy 0070 or FDA requirements is valuable. Excellent attention to detail, communication skills, and a collaborative mindset help ensure accurate and effective data sharing. These skills and qualities are vital for ensuring transparent, compliant, and responsible dissemination of clinical trial data while protecting patient privacy.

What are some typical challenges faced in a Clinical Trial Data Transparency role?

Professionals in Clinical Trial Data Transparency often navigate complex regulatory requirements and tight deadlines to ensure timely data disclosure while safeguarding participant confidentiality. You may face challenges related to interpreting evolving global regulations, coordinating across international teams, and handling large volumes of sensitive data. Collaboration with legal, regulatory, and data management teams is common, so strong communication and organizational skills are essential. By effectively managing these challenges, you play a crucial role in upholding ethical standards and public trust in clinical research.

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Clinical Trial Data Transparency jobs near you
Infographic showing various Clinical Trial Data Transparency job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.
Clinical Trial Associate

Clinical Trial Associate

Integrated Resources INC

Woodcliff Lake, NJ • On-site

$35.50 - $48.50/hr

Other

Posted 20 days ago

Job description

Company Description

At Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include- applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective

All in all, our expertise lies in providing trained and committed minds to help meet your business objectives, irrespective of the stage your business is in.

Job Description

Job Title: Clinical Trials Disclosure Associate
Duration: 1 year+
Location : Woodcliff Lake, NJ
JOB DESCRIPTION:
The Clinical Disclosure Associate will work across multiple disciplines within and outside Regulatory Affairs to drive departmental and project objectives.
Person will be responsible for coordinating the posting of registration and disclosures on clinicaltrials.gov, EudraCT and other registries for company-wide studies.
This comprises supervision of the vendor as well as coordination of company internal processes to ensure compliance with all relevant legal obligations (primarily clinicaltrials.gov and EudraCT disclosure).
Must be database proficient with registrations and disclosures.
Has the ability to work cross-functionally and meet required deadlines.
Ensures trial disclosure is in compliance with applicable regulations globally.
Develops and maintains strong internal relationships across all levels of the clinical organization.
Escalates issues to management in an expedient manner.
Continually train and remain in compliance with all current industry requirements as they relate to clinical trial disclosures.
On occasion, responsibilities may be extended to:- reviews of clinical and regulatory documents and regulatory submissions for data accuracy, consistency, formal quality and readability, resolving identified issues in collaboration with authors in a productive fashion
Coordinates all Client clinical disclosure activities, acting as primary intermediary between the disclosure vendor and Client contacts 30Works with Client contacts to identify and resolve compliance gaps 30
Supports continual improvements by evaluating disclosure business process, suggests and implements improvements to enhance compliance, documents processes and trains relevant personnel 20
Maintains Client disclosure trackers and produces metrics reports for management 10Maintains Client product information for use in disclosure activities 10.
REQUIREMENTS:
Bachelor's degree required.
Atleast 3 years working in the pharmaceutical industry in an R&D environment.
Solid knowledge of clinical trial transparency principles, preferably on an international level
Strong attention to detail and the ability to work as a part of a team across multiple departments
Strong communication and influencing skills.

Additional Information

Regards,

Pooja Mishra,

732-243-0715

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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