Clinical Studies Specialist

Description Home Search Jobs Job Description Clinical Studies SpecialistContract: North Chicago, Illinois, USSalary Range: 25.00 - 30.00 | Per HourJob Code: 368657End Date: 2026-05-13 Days Left: 27 days, 4 hours leftApplyPosition Details: Client: Pharmaceutical CompanyPosition Title: Clinical Studies Specialist IIDuration: 12 months (Possible extension)Location: North Chicago, IL 60064 (Hybrid)Pay Range: $25/hr to $30/hrTop 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 PhoneAnwesha Mohapatra anwesha.mohapatra@ Apply Now

Created: 2026-04-18