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Clinical Trial Safety Associate Jobs (NOW HIRING)

Clinical Trial Assistant / Clinical Study Associate * Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like:

Clinical Trial Associate II

Cambridge, MA ยท On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... Safety Letter distribution, Confidentiality Agreements and Clinical Trial Contracts, as well as ...

Clinical Trial Assistant / Clinical Study Associate * Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like:

Clinical Trial Specialist

Cincinnati, OH ยท On-site

$32.25 - $44/hr

... in their safety and effectiveness, and supports better experiences and outcomes for healthcare ... Works with, collaborates with and may oversee Clinical Research Associates (CRAs). * Ensure site ...

Clinical Trial Specialist

Cincinnati, OH ยท On-site

$32.25 - $44/hr

... in their safety and effectiveness, and supports better experiences and outcomes for healthcare ... Works with, collaborates with and may oversee Clinical Research Associates (CRAs). * Ensure site ...

Clinical Trial Assistant / Clinical Study Associate * Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like:

Clinical Trial Assistant / Clinical Study Associate * Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like:

Clinical Trial Specialist

Cincinnati, OH ยท On-site

$32.25 - $44/hr

... in their safety and effectiveness, and supports better experiences and outcomes for healthcare ... Works with, collaborates with and may oversee Clinical Research Associates (CRAs). * Ensure site ...

Clinical Trial Assistant / Clinical Study Associate * Clinical Research Associate * Clinical Research Specialist / Clinical Trial Manager * Clinical Program Manager What the work looks like:

$165K - $204K/yr

Support clinical trial safety activities, including review of aggregate safety data, safety listings, relevant safety analyses, and clinical trial safety documentation. * Collaborate with Clinical ...

Showing results 21-40

Clinical Trial Safety Associate information

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$17

$39

$70

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

As of Sep 13, 2026, the average hourly pay for clinical trial safety 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 popular job titles related to Clinical Trial Safety Associate jobs?

For Clinical Trial Safety Associate jobs, the most frequently searched job titles are:

Clinical Trial Manager

Sonoma, CA โ€ข On-site

Other

Posted 9 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