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Clinical Trial Transparency Manager Jobs (NOW HIRING)

Procter & Gamble

Clinical Trial Manager

Mason, OH · On-site

A P&G Clinical Trial Manager will be responsible for: * Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key ...

TransMedics

Clinical Trial Manager

Andover, MA · On-site

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 ...

MD Anderson

Clinical Trial Laboratory Manager

Houston, TX · Hybrid

$56.97 - $68.27/hr

The Clinical Trial Laboratory Manager provides leadership and oversight for all clinical trial laboratory operations, ensuring alignment with institutional goals, regulatory compliance, and best ...

MD Anderson

Clinical Trial Laboratory Manager

Houston, TX · Hybrid

$56.97 - $68.27/hr

The Clinical Trial Laboratory Manager provides leadership and oversight for all clinical trial laboratory operations, ensuring alignment with institutional goals, regulatory compliance, and best ...

Tango Therapeutics

Clinical Trial Leader

Boston, MA · Hybrid

Manage trial budgets, change orders, and invoice reconciliation in collaboration with vendor ... Oversee database lock, clinical study report (CSR) development, and study close-out activities.

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 ...

MD Anderson

Clinical Trial Laboratory Manager

Houston, TX · Hybrid

$56.97 - $68.27/hr

The Clinical Trial Laboratory Manager provides leadership and oversight for all clinical trial laboratory operations, ensuring alignment with institutional goals, regulatory compliance, and best ...

MD Anderson

Clinical Trial Laboratory Manager

Houston, TX · Hybrid

$56.97 - $68.27/hr

The Clinical Trial Laboratory Manager provides leadership and oversight for all clinical trial laboratory operations, ensuring alignment with institutional goals, regulatory compliance, and best ...

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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 Manager

Summit Therapeutics

Palo Alto, CA • On-site

Full-time

Posted 29 days ago

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Overview of Role:
The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Responsible for study start up and maintenance through study close out. Coordinates, leads and drives leads Summit cross functional team members, CROs and vendors to successfully deliver clinical studies. Responsible for all performance metrics and quality of deliverables in the clinical trial.
Role and Responsibilities:
  • Oversees study scope, quality, timelines, and budget with the internal Summit functional leads, CRO and vendors to ensure that overall project objectives are met
  • Initiates and builds solid professional relationships with key opinion leaders and clinical site staff
  • Partners with the CRO to ensure robust patient enrollment strategies are developed and carried out effectively to ensure patient enrollment is completed on time
  • Partners with the CRO to ensure robust ongoing data monitoring strategies are developed and carried out effectively to ensure delivery of high-quality data
  • Proactive identification and management of study related risks
  • Responsible for the development and management of clinical trial documents including (but not limited to) protocols, Case Report Forms (CRFs), consent documents, confidentiality agreements
  • Responsible for reviewing and managing study related plans, processes including
  • Investigator agreements (CTA), CRFs, CRF guidelines, statistical / pharmacokinetic analysis plans, monitoring plan, data management, safety monitoring
  • Responsible for reviewing CRO and vendor contracts/work orders and specifications to enable study objectives to be met
  • Reviews and approves essential document packages to enable timely site activations
  • Reviews pre-study, study initiation, interim monitoring visit and at study closeout visit report
  • Provides close oversight on the findings on the monitoring reports and loops back with broader team to provide updates
  • Directs investigator performance and adherence to protocol, and proactively addresses conduct issues and enrollment problems, as necessary
  • Responsible for oversight on the maintenance of the TMF and completeness at the end of the study
  • Perform periodic QC of the TMF
  • Oversee the creation and execution of clinical trial activities in accordance with Good Clinical Practices. Ensure compliance of clinical trials with national and international regulatory requirements and co-monitoring the assigned clinical trial following company SOPs
  • Ensures the study is "inspection ready" always
  • Responsible for oversight and coaching of the functional activities of Clinical Trial Associates allocated to the project
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:
  • Bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred
  • 5+ years of clinical project management experience in conducting international clinical trials in sponsor Pharma/Biotech organization
  • Prior phase II and III experience required
  • A solid understanding of the drug development process, ICH guidelines/GCP and specifically, each step within the clinical trial process
  • Experience with budget forecasting and management
  • Experience with clinical studies in oncology
  • Ability to travel internationally to visit clinical sites and for study meetings. Amount will vary upon project needs (up to 20%)
  • Proven proficiency in overseeing large complex studies being managed in house and by a CRO
  • Demonstrated ability to lead teams and work in a fast-paced team environment
  • Experienced and enjoys building relationships with KOLs and site personnel
  • Ability to successfully engage and work collaboratively with overseas clinical operations team members/colleagues
  • Demonstrated ability to build and deliver on patient enrollment strategies
  • Excellent interpersonal and decision-making skills. Demonstrates innovation, possesses drive, energy, and enthusiasm to deliver the program objectives
  • Demonstrated ability to comprehend complex scientific concepts and data
  • Proficient in reviewing and assessing clinical data
  • Possesses excellent planning, time management & coordination skills
  • Demonstrated ability to problem solve and use clear judgment in relation to regulatory requirements, interactions with external parties, timelines, and complex clinical programs
  • Experience in working in a small organization
  • Excellent written and oral communication skills

This is the pay for this position
Pay Transparency
$140,000-$150,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

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