Clinical Studies Specialist at Collabera

Position Clinical Studies Specialist
Posted 06 Aug 2026
Expired 05 Sep 2026
Company Collabera
Location North Chicago | US
Job Type Full Time

Job Description:

Latest job information from Collabera for the position of Clinical Studies Specialist. If the Clinical Studies Specialist vacancy in North Chicago matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Collabera for the position of Clinical Studies Specialist below matches your qualifications.

Position Details

Client: Pharmaceutical Company
Position Title: Clinical Studies Specialist II
Duration: 06 - 12 months (Possible extension)
Location: North Chicago, IL 60064 (Hybrid)
Pay Range: $25/hr to $30/hr

Top Skills
  • Strong attention to detail and accuracy
  • Proficiency with computers and ability to quickly learn new systems
  • Data entry and document review experience
  • Strong organizational, time management, and prioritization skills
  • High school diploma or equivalent; BA/BS degree preferred in Science, English, Business or related field
Description

This contractor position supports the creation, transfer, review, and coordination of clinical labels for clinical supplies used in clinical studies. The role requires exceptional attention to detail, strong computer proficiency, and the ability to quickly learn and apply new systems and processes. A high degree of accuracy in data entry and document handling is essential.

This position operates in a highly regulated environment and requires excellent organizational and time management skills, strong written and verbal communication skills, and the ability to follow detailed instructions and established processes. The successful candidate must be dependable, self-motivated, able to work independently, and also function effectively as part of a team. The ability to adjust priorities on short notice in response to changing business needs is critical.

Key Responsibilities
  • Transfer clinical labels into a new system
  • Create and design clinical labels according to established requirements
  • Proofread label proofs to ensure accuracy and compliance
  • Coordinate labeling documentation and related approvals
  • Support additional labeling-related projects as needed
Additional Responsibilities
  • Manage assigned labels and studies independently
  • Create labels using source documents and global regulatory requirements, ensuring information is complete, consistent, and accurate
  • Communicate and coordinate labeling and documentation activities with worldwide affiliates
  • Maintain professional communication with internal business partners and global stakeholders
Qualifications
  • Proficient computer skills and ability to quickly learn new software and systems
  • Data entry experience with a high degree of accuracy
  • Strong attention to detail and organizational skills
  • Excellent written and verbal communication skillsAbility to work independently with minimal supervision
  • Ability to collaborate effectively as part of a team
  • Strong time management skills and ability to manage multiple priorities
  • Comfortable working in a highly regulated environment
  • Able to follow detailed instructions and established procedures
  • Flexible and responsive to changing priorities and business needs
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, longterm disability insurance, shortterm 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 AS Applicable)

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Job Info:

  • Company: Collabera
  • Position: Clinical Studies Specialist
  • Work Location: North Chicago
  • Country: US

How to Submit an Application:

After reading and understanding the criteria and minimum qualification requirements explained in the job information Clinical Studies Specialist at the office North Chicago above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.

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