Labeling Specialist

Job Description: Clinical Labeling Support Specialist Location: Waukegan Road, North Chicago, IL 60064 Duration: 6–12 months (Based on performance and business needs) Work Environment: Highly Regulated / GMP Environment Position Overview: The Clinical Labeling Support Specialist will support the Clinical Labeling Team in creating, designing, reviewing, and proofreading clinical study labels for clinical supplies in a highly regulated Good Manufacturing Practice (GMP) environment. A primary focus of this role will be assisting the team with a major system transition by migrating label information between systems. The ideal candidate must possess exceptional attention to detail, strong computer proficiency, and high-accuracy data entry skills. Direct clinical labeling experience is a bonus, not required , as training will be provided; however, candidates must demonstrate the ability to learn new software applications quickly and work independently in a fast-paced environment. Qualifications & Skill Requirements: Required Qualifications: Education: High School Diploma or Equivalent required; Associate’s or Bachelor’s degree in Science, English, Business, or a related field preferred. (Note: Candidates with a Master's degree will be considered, but must be aligned with a foundational, hands‑on role). Data Entry & Accuracy: Proven experience performing high-volume data entry with outstanding precision and zero tolerance for error. Computer Proficiency: Strong overall technical/computer skills with a demonstrated ability to learn new software, systems, and tools rapidly. Regulated Environment Experience: Background working within a GMP (Good Manufacturing Practice) or highly regulated environment, following strict SOPs and compliance standards. Technical Software: Proficiency in Microsoft Excel and tracking/intake tools like Smartsheet . Design Tools: Familiarity with label design software or non-Adobe graphic design software is a plus. Analytical Mindset: Prior experience reviewing analytical documentation, source documents, or clinical trial protocols. Relevant Roles: Experience as a Clinical Research Coordinator, Document Control Specialist, Quality/Regulatory Documentation Support, or Data Entry Specialist in pharma/biotech. Key Responsibilities: Data Migration & System Support: Assist with transitioning label data from a legacy system to a new labeling system with a high level of precision. Label Proofreading & Quality Control: Perform meticulous proofreading of clinical label proofs to ensure 100% accuracy, including characters, multi-country/multi-language text, and regulatory compliance. Label Design & Creation: Design and create clinical labels according to established specifications, protocols, and regulatory requirements. Documentation & Process Execution: Follow Standard Operating Procedures (SOPs), interpret clinical protocols, and utilize source/analytical documentation to build accurate label content. Workflow & Coordination: Manage and track assigned label tasks using tools like Smartsheet and Microsoft Excel, ensuring no mix-up of information across multiple concurrent projects (high-volume workload). Communication: Coordinate labeling activities and documentation with global affiliates, project managers, and internal stakeholders. Key Competencies & Success Factors Attention to Detail: Absolute accuracy in reviewing characters, symbols, and text across foreign languages. Time Management & Multitasking: Ability to handle a high workload across multiple active studies without mixing up project details. Adaptability & Fast Learner: Quick to absorb training on complex software systems and operate independently in the short term. Reliability & Communication: Clear written/verbal communication skills and a strong sense of accountability in a collaborative team setting. At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. #J-18808-Ljbffr SPECTRAFORCE