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Clinical Studies Specialist II

Spectraforce Technologies
United States, Illinois, North Chicago
Aug 03, 2026
Location: AP15 - Lake County - Hyrbid Required M/F Remote - T/W/TH Onsite - Non-negotiableContract: 6-12 months - based on performance and business needsWhat are the top 3-5 skills, experience or education required for this position:1.Strong attention to detail and accuracy2.Proficiency with computers and ability to quickly learn new systems3.Data entry and document review experience4.Strong organizational, time management, and prioritization skills5.High school diploma or equivalent; BA/BS degree preferred in Science, English, Business or related fieldSuggested Title: Clinical[strong data-ogsc=""]Labeling Support Specialist Job 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 ResponsibilitiesTransfer clinical labels into a new systemCreate and design clinical labels according to established requirementsProofread label proofs to ensure accuracy and complianceCoordinate labeling documentation and related approvalsSupport additional labeling-related projects as neededAdditional Responsibilities, if the Contractor Proves SuccessfulManage assigned labels and studies independentlyCreate labels using source documents and global regulatory requirements, ensuring information is complete, consistent, and accurateCommunicate and coordinate labeling and documentation activities with worldwide affiliatesMaintain professional communication with internal business partners and global stakeholdersQualificationsProficient computer skills and ability to quickly learn new software and systemsData entry experience with a high degree of accuracyStrong attention to detail and organizational skillsExcellent written and verbal communication skillsAbility to work independently with minimal supervisionAbility to collaborate effectively as part of a teamStrong time management skills and ability to manage multiple prioritiesComfortable working in a highly regulated environmentAble to follow detailed instructions and established proceduresFlexible and responsive to changing priorities and business needs Enable Skills-Based Hiring No Provide the days of the week and the hours that this position will require: (No Value)
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