ZipRecruiter

Log In

1

Clinical Trial Data Transparency Jobs (NOW HIRING)

City of Hope

Sr Clinical Trials Data Coord

Duarte, CA · On-site

Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...

Aerogen Pharma Limited

$120 - $170/hr

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... This includes vendor management, monitoring subject safety and data collection, and ensuring ...

New

Clinovo

Clinical Trial Manager

Waltham, MA · On-site

The Role The Clinical Trial Manager (CTM) will be a key contributor to the successful execution of ... Partner closely with Data Management, Biostatistics, Regulatory Affairs, Pharmacovigilance, and ...

Recor Medical

Clinical Programmer II

Palo Alto, CA · On-site

Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational ...

Skyhawk Therapeutics

Clinical Trial Manager

Waltham, MA · On-site +1

$140K - $200K/yr

Ability and willingness to travel up to 25% of time Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Manager is ...

C4 Therapeutics Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

Perform and contribute to clinical data cleaning as part of cross-functional data review team ... Preferred: * Experience with oncology clinical trial management and/or global clinical trials.

Recor Medical

Clinical Programmer II

Palo Alto, CA

Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... This includes vendor management, monitoring subject safety and data collection, and ensuring ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of ... Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86 - $105/hr

Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ... Experience with clinical trial systems such as EDC, CTMS and eTMF platforms, preferred.

previous page

Showing results 41-60

All JobsHealthcare JobsClinical Trial Data Transparency Jobs

Clinical Trial Data Transparency information

See salary details

$13

$38

$86

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

As of Sep 4, 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?

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 skills and qualifications are needed for clinical trial data transparency?

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.

More about Clinical Trial Data Transparency jobs

What cities are hiring for Clinical Trial Data Transparency jobs?

Cities with the most 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 job categories do people searching Clinical Trial Data Transparency jobs look for?

The top searched job categories for Clinical Trial Data Transparency jobs are:

Clinical Trial Data Transparency jobs near you
Infographic showing various Clinical Trial Data Transparency job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 4% Temporary, and 4% Contract. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Clinical Trial Associate

Integrated Resources INC

Woodcliff Lake, NJ

$35.50 - $48.50/hr

Full-time

Re-posted 15 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

View All Integrated Resources Jobs

Apply