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Clinical Trial Transparency Associate Jobs (NOW HIRING)

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research projects, working with the study team in the initiation, maintenance and closeout of clinical projects ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA

$35.50 - $48.50/hr

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma. The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial.

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 ...

Sumitomopharma

Clinical Trial Associate

Marlborough, MA · On-site

$34.75 - $47.50/hr

Scope: The Clinical Trial Associate (CTA) plays a key role in supporting the operational and regulatory execution of clinical trials, acting as a central resource to study teams, and handling ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$35.50 - $48.50/hr

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma. The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial.

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 ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA · On-site

$90K - $110K/yr

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma. The CTA is responsible for executing the tasks on the clinical team throughout the clinical trial.

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

For Associate CTM: Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or ...

Sironax

Clinical Trial Associate (CTA)

Waltham, MA · On-site

$36.25 - $49.25/hr

Clinical Operations Reports To: VP of Clinical Operations Position Summary The Clinical Trial Associate (CTA) plays a critical role in the successful execution of Sironax clinical trials across Phase ...

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

Our mission is to bring innovation to clinical trial execution through passion, transparency, co ... Clinical Operations Associate: $70,304 - 80,000 annually + benefits package and annual performance ...

Crinetics Pharmaceuticals

Clinical Trial Associate

$34.25 - $46.75/hr

The Clinical Trial Associate ("CTA") is a highly skilled specialist contributing to the development of relevant concepts, techniques and processes by assisting and helping lead the study team across ...

Immatics NV

Clinical Trial Manager

Houston, TX

$130K - $150K/yr

Associate Director, Team Lead Site Operations Location :FullyRemote Salary Range: $130,000 - $150 ... Proficiencywith clinical trial systems and tools (e.g., CTMS, eTMF, Microsoft Office ...

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Clinical Trial Transparency Associate information

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

As of Jul 3, 2026, the average hourly pay for clinical trial transparency associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What are Clinical Trial Transparency Associates?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are some typical challenges faced by a Clinical Trial Transparency Associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.
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Clinical Trial Transparency Associate jobs near you

Clinical Trial Associate II

Kailera Therapeutics, Inc.

Waltham, MA

$36.25 - $49.25/hr

Other

Posted 14 days ago

Job description

What You'll Do:

The Clinical Trial Associate II will provide support to the Director of Clinical Operations in the conduct of trials and may be responsible for managing startup activities, vendor communication, internal meetings, or other project activities, as assigned. They will perform work within established protocols under general supervision, established processes, and regulations. 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Assists with preparation of all external and internal documentation for assigned trials, to ensure such documentation is completed in accordance with ICH GCP requirements and is consistent with the study protocol, under close supervision
  • Supports Clinical Trial Manager(s) in site management activities, which could include review of monitoring visit reports, communication with monitors and sites, review of site essential regulatory documents, and other activities as assigned
  • Manages and regularly updates clinical trial tracking tools and systems that provide metrics and tracking of a clinical trial's progress, including participant recruitment, trial supplies, lab samples, and participant disposition
  • Maintains and tracks revisions to clinical trial documentation for accuracy, including participant Informed Consent Forms and study plans
  • Prepares and/or reviews meeting minutes for cross-functional study team meetings
  • Assists the Clinical Trial Manager in ensuring compliance with Clinical Study Protocol(s) and provides timely updates
  • Organizes and prepares study files for submission to the Trial Master File within established guidelines
  • Responsible for tracking internal study team training, and managing training requirements
  • Tracks delivery and receipt of required supplies and materials to study sites and provides regular status updates
  • Performs other duties as assigned

Required Qualifications:

  • 2-5 years of relevant experience in a pharmaceutical/biotechnology or CRO environment, or academic research
  • Has a basic understanding of ICH GCP regulations and clinical protocols
  • Exhibits ability to 'multi-task' effectively
  • Ability to interact well with various team members and provide value added support to projects
  • Displays ability to independently solve routine problems following standard policies/procedure
  • Proficient computer skills using Microsoft Word, Excel, PowerPoint, etc.
  • Strong interest in clinical trials and initiative to learn and participate in projects of increasing responsibility
  • Strong organization and communication skills

Education:

  • BS/BA, Life Science degree is a plus

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