Clinical Trial Associate

Integrated Resources INC

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Lexington, MA, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job description

IRI believes in commitment, integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.


We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.


Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.

Job Title: Clinical Trial Associate 

Location: Lexington, MA

Duration: 3 Months +


Job Summary:

Responsible for assisting and providing support to the members of the clinical operations project team (i.e. Clinical Project Managers, Associate Directors, or Directors), in order to facilitate the management of pre- and post-approval clinical trial processes including quality review and document prep. The CTA performs work within established protocols under general supervision. 


Responsibilities:

• Main priority is candidate is competent and able to do this role, and start ASAP. 

• Candidate needs to be able to jump in and do work well. 

• Candidate will be working on documentation review in QC. 

• Candidate must understand clinical trial process and documentation. 

• Must have SOME experience in clinical trial process and documentation. 

• Willing to see new graduates as long as they have some experience.


 Must have SOME experience in clinical trial process and documentation. 


• Willing to see new graduates as long as they have some experience.

Amrit Singh

Clinical Recruiter

Integrated Resources, Inc.

IT REHAB CLINICAL NURSING

Tel: (732) 429 1634 (Direct)

Ext: (732) 549 2030 x (212) 

Fax: (732) 549 5549

http://www.irionline.com

Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012, 2013 & 2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

https://www.linkedin.com/company/46970?trk=prof-exp-company-name


About this role

Summary

Assist clinical team with trial documentation, quality review, and process support.

Job title

Clinical Trial Associate

Experience level

some experience

Industry

healthcare

Location requirements

Lexington, MA, on-site; remote not specified

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

clinical trial processdocumentation

Preferred skills

None specified

Specializations

clinical trial processdocumentationquality review
Locations

Structured locations inferred from the posting.

Lexington, MA, USA

On-site City