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Clinical Trial Study Assistant Jobs (NOW HIRING)

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

The Clinical Trial Assistant will play a key role to provide operational support to coordinate the ... Support clinical study manager with study budget tracking and payments of clinical sites and ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Track study progress and generate routine status reports and metrics as requested * Assist with ...

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... Track study progress and generate routine status reports and metrics as requested * Assist with ...

Socket.dev

Clinical Trial Assistant

Redwood City, CA · On-site

$90K - $108K/yr

Working with cross functional study teams, and vendors to assist in the coordination of clinical trial activities. * Support other clinical operations activities as appropriate. Required Skills ...

Alpha-9 Oncology

Clinical Trial Manager

Boston, MA · On-site

Support forecasting and management of clinical trial supplies (e.g., lab kits) to ensure sites have the materials needed to conduct studies. * Assist in the preparation of Investigator and Study ...

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

The Clinical Trial Assistant will play a key role to provide operational support to coordinate the ... Support clinical study manager with study budget tracking and payments of clinical sites and ...

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65K - $85K/yr

The Clinical Trial Administrator (CTA) fulfils a specialized research role within the Clinical ... study-specific source documentation, regulatory binders and other materials * Assist principal ...

Worldwide Clinical Trials

Clinical Trial Liaison

The Clinical Trial Liaison will also assist with the overall remit for Scientific Solutions ... Work closely with internal study teams and sites to foresee and proactively manage study site ...

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

The Clinical Trial Assistant will play a key role to provide operational support to coordinate the ... Establish, organize and maintain electronic study files and trial master files, with CRO as ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

The Clinical Department is responsible for executing clinical studies in full compliance with ... . * Assist with CRA and third-party vendor training on protocols and practices. * Develop and ...

Intuitive

Clinical Trial Assistant

Sunnyvale, CA

$70K - $94K/yr

The Clinical Trial Assistant will play a key role to provide operational support to coordinate the ... Establish, organize and maintain electronic study files and trial master files, with CRO as ...

Aerogen Pharma Limited

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... readiness. * Assist in the development of study documents and tools including informed consent ...

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Clinical Trial Study Assistant information

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How much do clinical trial study assistant jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical trial study assistant in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What cities are hiring for Clinical Trial Study Assistant jobs?

Cities with the most Clinical Trial Study Assistant job openings:

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Infographic showing various Clinical Trial Study Assistant job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 74% Full Time, 18% Part Time, and 5% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Study Assistant

New Brunswick, NJ • On-site

Motion Recruitment Partners, LLC
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Motion Recruitment Partners, LLCexternal

Other

Medical, Dental, Vision, Retirement, PTO

Posted 25 days ago

Job description

Clinical Study Assistant
Kelly Science and Clinical FSP is currently seeking a Clinical Study Assistant (CSA) for a long-term engagement with one of our Global Medical Device clients. This position is remote in eastern time zone. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation, and sick/personal time.
Summary:
CSA is responsible for processing, tracking, and filing of study documents, and management of the Trial Master File within the clinical projects. In addition, administratively support clinical study staff as required. Supports project managers within the assigned clinical studies.
Deliverables:
  • Work with Study Teams and partners to maintain and track relevant activities in CTMS.
  • Creation/distribution of regulatory binders
  • Timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions.
  • Distribution of safety documentation to other functional groups in support of safety committee meetings as requested (supporting role).
  • Creation and generation of system reports.
  • Provide support for study supplies creation, ordering and distribution to the sites e.g. print protocols, burn DVDs
  • Assist with Medical Device tracking and ordering if required and if applicable.
  • Metrics/KPIs:
  • Metrics/KPIs governing these services are outlined in the QOP document.
Education and Experience Guidelines:
  • Minimum of a Bachelor's Degree is preferred
  • Previous clinical research experience a plus.
  • Requires previous administrative support experience or equivalent for at least 1 year.
  • Clinical/medical background a plus.
  • Requires experience and knowledge working with computer systems (Microsoft office - Excel, Word and Power Point).

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