ZipRecruiter

Log In

1

Clinical Trial Disclosure Jobs (NOW HIRING)

Ipsen

Clinical Trial Administrator

Cambridge, MA · On-site

Clinical Trial Administrator Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid ... EFPIA disclosure code (Europe), Sunshine Act (US): * Collect all the information related to ...

Ionis

Clinical Trial Management Associate

Carlsbad, CA · On-site +1

$34.50 - $47.25/hr

The Clinical Trial Management Associate (CTMA) works as part of the Study Management Team to ... Disclosure Agreements (CDAs), contracts, proposals, invoices, and other study documentation

next page

Showing results 1-20

All JobsClinical Trial Disclosure Jobs

Clinical Trial Disclosure information

See salary details

$11

$37

$68

How much do clinical trial disclosure jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for clinical trial disclosure in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Trial Disclosure Specialist, you need a solid understanding of clinical research, regulatory compliance, and scientific writing, often supported by a degree in life sciences or a related field. Familiarity with disclosure platforms like ClinicalTrials.gov, EudraCT, and document management systems, as well as knowledge of global regulatory guidelines, is essential. Attention to detail, organization, and effective communication are vital soft skills for managing complex data and coordinating with cross-functional teams. These skills ensure accurate, timely, and compliant disclosure of clinical trial information, maintaining transparency and supporting regulatory requirements.

What is the difference between Clinical Trial Disclosure vs Clinical Research Coordinator?

AspectClinical Trial DisclosureClinical Research Coordinator
Primary RoleProviding information about clinical trials to the public and regulatory bodiesManaging and coordinating clinical trial activities at research sites
Required CredentialsKnowledge of regulations, medical writing, and complianceOften requires a degree in health sciences, certification in clinical research
Work EnvironmentRegulatory agencies, pharmaceutical companies, research organizationsHospitals, research sites, clinical trial sites

While Clinical Trial Disclosure focuses on communicating trial information to ensure transparency and compliance, Clinical Research Coordinators handle the day-to-day management of clinical trials at research sites. Both roles require knowledge of clinical research processes, but their responsibilities and work environments differ significantly.

What are some common challenges faced by professionals in Clinical Trial Disclosure roles, and how can they be managed?

Professionals in Clinical Trial Disclosure often face challenges such as navigating complex global regulations, ensuring accuracy and timeliness of data, and coordinating with cross-functional teams. The evolving landscape of transparency requirements means staying updated on new legislation and sponsor obligations is essential. Effective communication, robust project management skills, and attention to detail help manage these challenges, while collaboration with regulatory, legal, and data management teams ensures disclosures meet both internal and external standards.

What is clinical trial disclosure?

Clinical trial disclosure refers to the process of making information about clinical trials publicly available, including trial registration, results, and other relevant data. This transparency is required by regulatory agencies to ensure ethical standards, promote scientific integrity, and provide information to patients and researchers. Disclosure often involves submitting trial details to public registries like ClinicalTrials.gov or the EU Clinical Trials Register, and sharing results even if they are negative or inconclusive.
More about Clinical Trial Disclosure jobs
What cities are hiring for Clinical Trial Disclosure jobs? Cities with the most Clinical Trial Disclosure job openings:
What are the most commonly searched types of Clinical Trial Disclosure jobs? The most popular types of Clinical Trial Disclosure jobs are:
What states have the most Clinical Trial Disclosure jobs? States with the most job openings for Clinical Trial Disclosure jobs include:
What job categories do people searching Clinical Trial Disclosure jobs look for? The top searched job categories for Clinical Trial Disclosure jobs are:
Clinical Trial Disclosure jobs near you
Infographic showing various Clinical Trial Disclosure job openings in the United States as of July 2026, with employment types broken down into 84% Full Time, 10% Part Time, 2% Temporary, and 4% Contract. Highlights an 85% In-person, 2% Hybrid, and 13% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.
Clinical Trial Transparency Senior Associate

Clinical Trial Transparency Senior Associate

Integrated Resources INC

Cambridge, MA

$36.50 - $50/hr

Other

Medical, Life

Posted 2 days ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Title: Clinical Trial Transparency Senior Associate

Location: Cambridge, MA
Duration: 7+ months (Possibility of extension)
Job Description:
Performs the Clinical Trial Registration and/or results disclosure activities for new and/or ongoing studies.
Ensures compliance due dates are defined and timelines are met.
Collaborates with the Study Team to complete the data entry in support of Clinical Trial Disclosure, utilizing information from source documents and systems (e.g. protocol, CTMS).
Assigns tasks, initiates workflows, follows up on all action required, and escalates alerts when needed in order to maintain content that has been made public (e.g. clinicaltrials.gov).
Shares accurate information with various functional leads to be utilized throughout global disclosures
Performs internal quality control review of disclosure information.
Participates in User-Acceptance Testing (UAT) of disclosure system.
Supports process analysis efforts by identifying opportunities to improve the efficiency and effectiveness of the Clinical Trial Disclosure process.
Generates metrics for disclosure activities.
Supports the development and delivery of training materials.
Requirements:
Firm understanding of Clinical Development and operations.
Previous experience (2-3 years minimum) in pharma/biotech industry.
Must have previous experience disclosing clinical trial information on ClinicalTrials.gov.
Minimum education of Bachelor Degree (or equivalent experience).
Experience with PharmaCM would be a plus.


Additional Information

We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

Thanks & Regards,


Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

DIRECT # - 732-844-8724|


LinkedIn: https://in.linkedin.com/in/seemachawhan
Gold Seal JCAHO Certified  for Health Care Staffing
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)

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