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Clinical Trial Transparency Manager Jobs (NOW HIRING)

Sagimet Biosciences

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor ...

TransMedics

Clinical Trial Manager

Andover, MA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end ... S. pay transparency laws and do not request or consider salary history. Employee Benefit: Medical ...

Entrada Therapeutics

Senior Clinical Trial Manager

Boston, MA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... clinical trial, including CRO and vendor management. * Support and manage various study activities ... We believe in transparency and equity and are committed to sharing salary ranges for every position ...

Parexel

Clinical Trial Leader

The CTL is responsible for managing the planning, implementation, and tracking of the clinical ... Makes effective use of resources, and proactively strives for transparency and clarity to ...

TransMedics

Clinical Trial Manager

Andover, MA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end ... S. pay transparency laws and do not request or consider salary history. Employee Benefit: Medical ...

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

The Clinical Trial Manager (CTM) plays a key role in the successful execution of clinical research studies, providing operational leadership from study initiation through final closeout. This ...

Collabera

Clinical Trial Manager

Jersey City, NJ

Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics. Demonstrated ability to support the development and management of ...

Kailera Therapeutics, Inc.

Clinical Trial Manager

Waltham, MA · On-site

$127K - $155K/yr

  • Medical

  • Life

  • Retirement

The Clinical Trial Manager will provide project support to team members by leading and/or participating in the daily management of clinical trial activities. Successful candidate will be working ...

Intuitive

Clinical Trial Manager

San Carlos, CA · On-site

The Clinical Trial Manager (CTM) will manage the day-to-day planning and execution of clinical studies to generate evidence supporting the safety, performance, and clinical utility of novel robotics ...

Biogen

Clinical Trial Manager

Cambridge, MA · Hybrid

$117K - $157K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

As a Clinical Trial Manager, you will be a vital part of the PO&T team within the Implantable Device Unit, supporting the planning, coordination, and execution of clinical studies. Your role is ...

New

Alpha-9 Oncology

Clinical Trial Manager

Boston, MA

  • Medical

  • Retirement

  • PTO

Manage day-to-day relationships with clinical trial vendors, including tracking vendor contracts, budgets, invoices, and payments against contracted scope of work, and escalating issues or variances ...

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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 Aug 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 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 skills and qualifications are needed to be a clinical trial transparency manager?

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
Infographic showing various Clinical Trial Transparency Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

Sagimet Biosciences

San Mateo, CA • On-site

$90 - $100/hr

Contractor

Re-posted yesterday

Job description

Job Type
Contract
Description
The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor activities and deliverables. Additional responsibilities include Independent oversight of outsourced clinical studies, protocol review for operational feasibility and consistency, CRO/vendor feasibility, request for proposal and bid defense process, country/site feasibility, tracking site selection, activation, and patient recruitment. The Clinical Trial Manager will also focus on the management of project timelines, relevant study plans (e.g. monitoring, study operations, quality, communications, etc.), EDC and IXRS set up and development and/or review of clinical data management conduct (e.g. eCRFs, CRF guidelines).
Essential Responsibilities:
• Clinical operations leader and main point of contact with counterpart at outside vendor, CRO and/or trial sites; daily review and identification of potential issues or problems and communicates/escalates to project team.
• Assist in the critical development and review of key study documents (e.g. Protocols, ICF, study plans eCRF, etc.).
• Develop, maintain and promote effective and collaborative working relationships with and among internal team members and external vendors and 3rd party personnel.
• Participate in Clinical Operations meetings as assigned.
• Lead reviews of key data to identify trends, discrepancies, errors etc. to ensure ongoing quality of conduct in accordance with the protocol and vendor contracts, including on-going review of emerging data for tables, listings, and figures.
• Work with junior CTM for oversight of in-house review of site monitoring reports and tracking to ensure appropriate monitoring of trial conduct and satisfactory resolution of outstanding issues.
• Work with junior CTM for oversight of Trial Master Files (TMF) oversight plan and laisses with CRO for annual quality check; ensuring tracking of ICH-GCP and/or FDA CRF21 essential study documents.
• Track patient and recruitment status using applicable spreadsheets and web portal tools.
• Assist in yearly IND updates including IBs and DSUR.
Requirements
• A minimum of a Bachelor's degree or equivalent is required, preferably in Life Sciences (e.g. Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
• A minimum of ten years clinical operations experience
• A minimum of three years of experience leading clinical trials from start-up to database lock
• Experience with all three parts of leading a global Phase 2 and/or Phase 3 clinical trial: start up, treatment phase and database lock.
• Experience in start up and oversight of central lab, including depth specification review.
• Knowledge of sample collect and analysis process at the study level and may perform reconciliation and/or tracking of sample manifests.
• Experience with data privacy and GDPR guidelines.
• Experience with the independent management and oversight of CROs/vendors required.
• Experience with double blind/placebo controlled studies required.
• Experience within a small biotech organization and flexibility to pivot quickly and think outside the box.
• Excellent attention to detail, accuracy in work and possesses strong analytical skills.
• Must think critically and creatively and be able to work independently to determine appropriate actions to resolve complex problems.
• Comprehensive knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials
Salary Description
$90-$100 per hour

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