Clinical Trials Associate II

Real Staffing

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Lexington, MA, us on site Until 8/21/2026 First posted March 26, 2025 Last posted March 26, 2025
Job description

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity.

To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com

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


  1. Main priority is candidate is competent and able to do this role, and start ASAP.
  2. Candidate needs to be able to jump in and do work well.
  3. Candidate will be working on documentation review in QC. 
  4. Candidate must understand clinical trial process and documentation.
  5. Must have SOME experience in clinical trial process and documentation. 
  6. Willing to see new graduates as long as they have some experience.

All your information will be kept confidential according to EEO guidelines. 

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 646-357-1104 ASAP!

I look forward to hearing from you!

About this role

Summary

Assist clinical trial teams with documentation, quality review, and process support under supervision.

Job title

Clinical Trials Associate II

Experience level

some experience

Industry

healthcare

Location requirements

on-site in lexington, ma, no remote work

Salary

Not specified

Management role

No

Skills & keywords

Required skills

clinical trial processdocumentationquality review

Preferred skills

None specified

Specializations

clinical trial processdocumentation reviewquality review
Locations

Structured locations inferred from the posting.

Lexington, MA, USA

On-site City