System Publisher II

Lab; Remote; GBP 30,000 - 40,000; Full time

Job summary

A leading contract research organization is seeking a detail-oriented System Publisher to support clinical trial processes. This remote position requires a scientific degree and two years of relevant experience, along with excellent communication and attention to detail. The role involves troubleshooting, document control, and collaborating with scientific teams to ensure accuracy in protocols. Opportunities for career development and competitive salaries are offered.

Benefits

Comprehensive training plan

Unsurpassed career development opportunities

Competitive salaries and benefits

Qualifications

• Two years of relevant experience in a related field.
• Experience as a chemist, study coordinator, or project manager.
• Strong competency with E-Workbook templates.
• Proficiency in Java, C#, or Visual Basic preferred.

Responsibilities

• Support the accuracy and integrity of clinical trial systems.
• Build templates and maintain document control for analytical procedures.
• Troubleshoot user issues and participate in process improvements.
• Assist users with the laboratory execution system support.

Skills

Excellent communication skills

Attention to detail

Time management

Knowledge of Microsoft Excel

Basic programming knowledge

Education

Scientific degree (BSc/MSc/PhD or equivalent)

Tools

E-Workbook

LIMS

Job description

About LabCorp:

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.

The Role:

We’re looking for a detail-oriented and adaptable System Publisher to join our team. In this role, you’ll 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 needs to be UK based.

Job 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
• Lab Execution System Support:
• Assists users with troubleshooting and escalating issues with the laboratory execution system.
• Demonstrates understanding in building templates
• Analytical Procedure Support
• Demonstrates understanding in document control of Bioanalytical Chemistry methods using electronic document control system.
• Uses the Method Procedure template.

What LabCorp Drug Development can offer you:

• 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 wide ranging projects.
• Competitive salaries and a comprehensive benefits package including health cover and contributory pension.

Education/Qualifications:

• Scientific degree (BSc/MSc/PhD or equivalent).

Experience:

• 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 (may be substituted with computer programming skills)
• 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

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

We encourage all to apply.

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