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Clinical Trial Transparency Jobs (NOW HIRING)

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the ...

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.

Seaport Therapeutics

Clinical Trial Manager

Boston, MA · On-site

$133K - $150K/yr

The Clinical Trial Manager (CTM) is responsible for leading the execution of clinical studies on ... CNS therapeutic experience strongly preferred At Seaport, we believe transparency and fairness are ...

Seaport Therapeutics

Clinical Trial Manager

Boston, MA · On-site

$133K - $150K/yr

The Clinical Trial Manager (CTM) is responsible for leading the execution of clinical studies on ... CNS therapeutic experience strongly preferred At Seaport, we believe transparency and fairness are ...

A-Line Staffing Solutions

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Clinical Trial Operations Specialist

Irvine, CA · On-site

$35 - $40/hr

... transparency reporting data to support Sunshine Act compliance. · Track, manage, and coordinate ... Clinical Trial Operations Specialist Requirements * Previous clinical trial experience is required.

New

Socket.dev

Clinical Trial Associate

Waltham, MA · On-site

$65 - $90/hr

We are seeking a Clinical Trial Associate (CTA) will work with the Clinical Study Lead and Director ... Additional Description for Pay Transparency: The final salary offered will depend on several ...

New

Innovo Research

Clinical Trial Recruiter

Champaign, IL · On-site

$19.25/hr

As a Clinical Trial Recruiter, you will play a pivotal role in advancing medical science by ... Vision Insurance COMPENSATION In the spirit of transparency, we are pleased to announce that the ...

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How much do clinical trial transparency jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical trial transparency 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 a clinical trial transparency?

A Clinical Trial Transparency job involves ensuring that information about clinical trials is publicly disclosed in compliance with global regulations and transparency policies. Professionals in this role manage the registration of trials on public databases, oversee the timely reporting of results, and ensure adherence to ethical and legal requirements. They collaborate with regulatory teams, medical writers, and legal departments to promote data accessibility and public trust in clinical research.

What are the main responsibilities in a clinical trial transparency role?

In a Clinical Trial Transparency role, your primary responsibilities include preparing and submitting clinical trial data and documents to public registries, ensuring compliance with global regulations, and responding to transparency-related inquiries from regulatory authorities. You’ll work closely with clinical teams, regulatory affairs, and medical writing staff to gather accurate data and ensure timely disclosures. The role often involves managing multiple projects simultaneously, staying updated on evolving disclosure regulations, and supporting audits or inspections. This position is essential in promoting openness, protecting patient privacy, and maintaining the integrity of clinical research.

What are the key skills and qualifications needed to thrive in a clinical trial transparency position, and why are they important?

Excelling in Clinical Trial Transparency requires a comprehensive understanding of clinical research protocols, regulatory compliance (such as FDA, EMA, and ICMJE requirements), and strong project management abilities. Familiarity with disclosure platforms (e.g., ClinicalTrials.gov, EudraCT), data anonymization tools, and relevant certifications like a GCP (Good Clinical Practice) certificate are highly valuable. Attention to detail, effective communication, and stakeholder management are crucial soft skills for success in this role. These capabilities ensure accurate, timely, and compliant disclosure of trial information, which is critical for regulatory approval and upholding public trust.

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Clinical Trial Transparency jobs near you
Infographic showing various Clinical Trial Transparency job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Associate

Skyhawk Therapeutics

Waltham, MA • On-site

$75K - $140K/yr

Full-time

Re-posted 12 days ago

Job description

Clinical Trial Associate/ Senior Clinical Trial Associate
Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations.
Responsibilities (including, but not limited to):
  • Organize, participate in, and maintain agendas and meeting minutes for all internal and cross-functional team meetings. Review external meeting minutes as required.
  • Work closely with our clinical operations team to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews).
  • Update and maintain internal trackers (e.g. central enrollment tracker, investigator engagement tracker, bioanalytical sample tracker) and implement updates into ad-hoc presentations and reports as required.
  • Maintain internal Clinical Operations study files and perform periodic reconciliations of documents to ensure all material is present and versioned correctly.
  • Create and maintain study personnel contact lists for all studies and KOLs by disease indication.
  • Assist with the review of study-related documents for clinical studies (e.g. protocol, IB, ICFs).
  • Assist with the facilitation of important external meetings (e.g. Clinical Advisory Board meetings): outreach, scheduling, execution of CDAs and contracts, travel arrangements, presentations, agendas, and minutes.
  • Assist with bioanalytical sample tracking and management of central and third-party labs (sample shipment and analysis timelines).
  • Assist with the review of central and third-party lab documents (e.g. Lab Manual, site flowcharts).
  • Assist with monitoring trip report across the program.

Requirements, Education, Experience & Skills:
  • Relevant education and training required; Bachelor's degree in administrative, science or medical areas of study is a plus.
  • At least 3-5 years of successful administrative experience in biotech/life sciences, health care or clinical study management (title commensurate with experience, with emphasis on eTMF experience)
  • Prefers to contribute as both independent, self-starter, and a collaborative team member.
  • Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment.
  • Excellent verbal and written communication skills.
  • Excellent computer skills, including Microsoft Office Suite: Calendar, Word, Excel, and PowerPoint are essential. SharePoint and SmartSheet preferred.
  • Veeva TMF working knowledge and for senior level, demonstrated knowledge of ICH-GCP, FDA and international regulatory requirements, eTMF management/oversight, and inspection readiness
  • Demonstrated multi-tasking and project management skills.

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.
About Skyhawk
Skyhawk is committed to discovering, developing and commercializing small molecule therapeutics that modify RNA expression. We use our novel SkySTAR® platform (Skyhawk Small molecule Therapeutics for Alternative splicing of RNA) to develop drug candidates directed toward targets for some of the world's most intractable diseases including neurological conditions, cancer, and traditionally "undruggable" targets.

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