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Clinical Trial Disclosure Associate Jobs (NOW HIRING)

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

... agreements, non-disclosure agreements, etc * Create purchase requests and process invoices ... Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ...

Actalent

Clinical Trial Associate - Hybrid

Philadelphia, PA · Hybrid

$33.75 - $46.25/hr

Clinical Trial Associate The Clinical Trial Associate (CTA) supports the Director of Clinical Operations and Clinical Study Managers in trial start-up, execution, and close-out activities while ...

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Support clinical trial registration and disclosure on websites per applicable regulatory requirements * Responsible for overall TMF status. Guide study team members on the eTMF/paper TMF document ...

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 ...

Summit Therapeutics

Sr. Clinical Trial Associate

Miami, FL · On-site

$32 - $43.75/hr

SENIOR CLINICAL TRIAL ASSOCIATE Location: ONSITE - Miami, FL Overview of Role: The Senior Clinical Trial Associate (Senior CTA) is an experienced clinical operations professional who is responsible ...

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

... agreements, non-disclosure agreements, etc * Create purchase requests and process invoices ... Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ...

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

... agreements, non-disclosure agreements, etc * Create purchase requests and process invoices ... Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical ...

StartX

Clinical Trial Associate

Redwood City, CA · On-site

$60 - $80/hr

The Clinical Trial Associate (CTA) supports CRAs, and study teams across Karius clinical studies by assisting with the collection, quality control, and quality assurance of study and trial related ...

Johnson and Johnson

Clinical Trial Specialist

Cincinnati, OH · On-site

$32.25 - $44/hr

Clinical Trial Support Job Category: Professional All Job Posting Locations: Cincinnati, Ohio ... Works with, collaborates with and may oversee Clinical Research Associates (CRAs). * Ensure site ...

Jobtailor

Clinical Trial Specialist

California, MO · On-site

$100 - $125/hr

Collaborate with and may oversee Clinical Research Associates. * Ensure site staff training and ... Document trial activities, write visit reports and follow-up letters, and communicate status and ...

New

Karius, Inc.

Clinical Trial Associate

Redwood City, CA · On-site

$60 - $80/hr

Position Summary The Clinical Trial Associate (CTA) supports CRAs, and study teams across Karius clinical studies by assisting with the collection, quality control, and quality assurance of study and ...

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

As of Sep 9, 2026, the average hourly pay for clinical trial disclosure 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 does a clinical trial disclosure associate do?

A Clinical Trial Disclosure Associate is responsible for preparing, reviewing, and submitting clinical trial information to public registries and databases, such as ClinicalTrials.gov and EudraCT. Their work ensures that clinical trial data is transparent and accessible to the public, regulatory agencies, and researchers. They collaborate with clinical teams, regulatory affairs, and legal departments to ensure compliance with global disclosure regulations. This role plays a crucial part in promoting transparency and trust in clinical research.

How does a clinical trial disclosure associate typically collaborate with other teams during the clinical trial process?

Clinical Trial Disclosure Associates work closely with clinical operations, data management, regulatory affairs, and medical writing teams to ensure all trial information is accurately and transparently reported. They coordinate with these groups to collect essential data, review protocols, and meet regulatory submission deadlines. Strong communication and organizational skills are essential, as the role often involves managing multiple concurrent projects and responding to evolving regulatory requirements. This cross-functional collaboration is key to maintaining compliance and supporting the overall success of clinical trial transparency initiatives.

What are the key skills and qualifications needed to thrive as a clinical trial disclosure associate, and why are they important?

To thrive as a Clinical Trial Disclosure Associate, you need a solid understanding of clinical research, regulatory requirements (such as FDA, EMA, or ICMJE guidelines), and a relevant life sciences degree. Familiarity with clinical trial registries (like ClinicalTrials.gov and EudraCT), document management systems, and regulatory submission platforms is crucial. Strong attention to detail, organizational skills, and effective collaboration and communication abilities distinguish top performers in this role. These skills ensure accurate, timely, and compliant public disclosure of clinical trial information, which supports transparency and regulatory adherence.

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Clinical Trial Disclosure Associate jobs near you
Infographic showing various Clinical Trial Disclosure Associate job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial Manager

Sunnyvale, CA • On-site

Elixir Associates
See more jobs at Elixir Associatesexternal

Other

Posted 5 days ago

Job description


Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program Manager


I am running a team build for a clinical-stage medical device company in the Bay Area! Early clinical results are in and positive; the trial programme is scaling, and they are building the clinical operations function out properly rather than hiring one person at a time.


Multiple hires, across levels:

  • Clinical Trial Assistant / Clinical Study Associate
  • Clinical Research Associate
  • Clinical Research Specialist / Clinical Trial Manager
  • Clinical Program Manager


What the work looks like: Operational ownership of investigational sites. Study start-up and activation, enrolment tracking, monitoring visits, TMF, query resolution, vendor and CRO coordination. Start-up through close-out, not one narrow slice of it. At the CPM end, programme-level oversight, timelines, budgets and cross-functional leadership.


Why people are taking this over a big-sponsor role

  • Equity
  • Career growth. Joining a function at build stage means the roles above you get created, not backfilled. Early hires here are positioned for the senior seats as the programme scales.
  • Leadership. An experienced clinical leadership team with prior device programmes behind them, and direct access to them from day one.
  • Breadth. You will not spend two years doing one task while someone else owns the study.
  • The technology. A genuinely novel approach in an indication affecting millions, with first-in-human data already in hand.


If any of these levels fit, message me or comment below


Tom Vos | Elixir Associates tom.vos@elixir-associates.com +1 646 631 1501

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