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Clinical Trial Transparency Manager Jobs (NOW HIRING)

Ipsen

Clinical Trial Administrator

Cambridge, MA · On-site

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 ...

millenniumsoft

Clinical Trial Assistant

Sparks, MD · On-site

Manage multiple activities and functions on a daily basis. * Study Product and Supply Inspection ... with Transparency (Sunshine) Act reporting, either by gathering data or with data entry. Other ...

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 ...

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 ...

4D Molecular Therapeutics

Clinical Trial Manager

The Clinical Trial Manager will support the Company's clinical trial activities. This position reports to the Director of Clinical Operations. This will be responsible for management of the day to ...

Galderma

Clinical Trial Manager

Boston, MA · On-site

Position Summary The Clinical Trial Manager (CTM) plans and manages overall activities for assigned global clinical trial(s). This includes timelines, budgets, resources, investigational sites ...

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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 Jun 15, 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
Clinical Trial Transparency Senior Associate

Clinical Trial Transparency Senior Associate

Integrated Resources INC

Cambridge, MA

$36.50 - $50/hr

Other

Medical, Life

Posted 19 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
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"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)

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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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