System Publisher II

Labcorp • Madison, WI

10h • $34 - $35 • Remote

About The Position

As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments. In this role, we’re looking for a detail-oriented and adaptable System Publisher to join our team. The incumbent will support the accuracy and integrity of systems and documentation that drive clinical trial processes. You’ll help troubleshoot issues, build templates, and maintain document control for analytical procedures. Working closely with scientific teams, you’ll ensure protocols, SOPs, and system templates meet quality standards. If you enjoy problem-solving, supporting users, and contributing to process improvements in a fast-paced environment, this is a great opportunity to make an impact. This is a fully remote position; however, the successful candidate will be based in the U.S.

Requirements

• Scientific degree (or equivalent).
• Two years of relevant experience, can include experience as a chemist, study coordinator, project manager, or equivalent with a BSc degree
• Excellent communication (verbal and written), presentation, and interpersonal skills.
• Excellent attention to detail.
• Efficient in prioritizing and managing time.
• Knowledge and use of Microsoft Office applications with an emphasis on MS Excel
• Established competency with E-Workbook templates (maybe substituted with computer programming skills)

Nice To Haves

• Experience with IDBS E-Workbook or a LIMS used in Bioanalytical or BioPharm CMC Chemistry preferred
• Working knowledge of computer programming languages (Java, C#, Visual Basic, etc.) preferred

Responsibilities

• Demonstrates proficiency in response to changing priorities and client needs without neglecting other responsibilities
• Demonstrates understanding in the role and accountability of System Publishing within Clinical Trial Testing Solutions.
• Participates in process improvement initiatives within the System Publishing team and associated business.
• Demonstrates understanding of the processes involved in the production of protocols, SOPs, analytical procedures, working documents, forms, reports, data evaluation and Client/QA audits.
• Demonstrates understanding of the principles, theories, and concepts of the scientific work that is being supported.
• Demonstrates understanding of processes designed to ensure templates for the laboratory execution system are accurate.
• Participates in system projects
• Supports user base by troubleshooting basic and complex issues
• Assists users with troubleshooting and escalating issues with the laboratory execution system.
• Demonstrates understanding in building templates
• Demonstrates understanding in document control of Bioanalytical Chemistry methods using electronic document control system.
• Uses the Method Procedure template.

Benefits

• A comprehensive training plan; with the ability to develop your technical and managerial skills.
• Unsurpassed career development opportunities.
• Ability to work with a variety of different clients on a wide range of projects.
• Competitive salaries, comprehensive benefits package including healthcare coverage and 401k plan.
• Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
• Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees