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Clinical Studies Specialist

Contract: North Chicago, Illinois, US

Salary Range: 25.00 - 30.00 | Per Hour

Job Code: 368657

End Date: 2026-05-13

Days Left: 19 days, 23 hours left

Position Details:
Client: Pharmaceutical Company
Position Title: Clinical Studies Specialist II
Duration: 12 months (Possible extension)
Location: North Chicago, IL 60064 (Hybrid)
Pay Range: $25/hr to $30/hr

Top 3 skills:

  • Bachelors or Masters degree with a Scientific focus
  • 3-5 years of pharmaceutical experience, preferably in a clinical trial environment
  • Ability to work independently and drive tasks to completion without high level of supervision

Education Requirement:

  • Bachelor’s Degree required preferably in physical science, math, engineering, pharmacy or data science.

Experience:

  • 3-5 years total experience in the Pharmaceutical Industry.

Major Responsibilities:

  • Planning, scheduling, coordination and execution, in support of clinical supply project manager to ensure the timely availability of investigational drug supplies and related services to clinical sites and depots.
  • Translates stability and packaging requests into an executed packaging design.
  • Identifies, develops, communicates and tracks task completion dates , activities, logistics, and milestones in support of clinical supply project manager to ensure the timely availability of investigational drug supplies
  • Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with the clinical supply project manager.
  • Responsible to complete tasks identified for the team.
  • Responsible for inventory management system set up activities (i.e. Material masters, manufacturing requests, etc) to support clinical packaging operations

Critical Success Factors:

  • A basic understanding of clinical development and global supply chain requirements.
  • Competent in the application of standard business requirements (for example SOPs, Global Regulations).
  • Understanding the importance of compliance in a regulated environment and be capable of applying this knowledge to daily work.
  • Ability to work collaboratively within the dept as well as cross-functionally including interacting in a tactful, professional and effective manner.
  • Ability to work effectively and professionally with those in the dept as well as QA,
  • Analytical and any area interface.
  • Ability to manage and prioritize multiple tasks.
  • Basic Project Management skills.
  • Good communication skills (both written and oral).

Benefits:
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually – These all are subject to applicable eligibility).

Job Requirement
  • clinical supply
  • clinical trial
  • drug supplies
Reach Out to a Recruiter
  • Recruiter
  • Email
  • Phone
  • Anwesha Mohapatra
  • anwesha.mohapatra@collabera.com
Apply Now
Apply Now
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