C

ClinChoice

Global CRO providing full-service clinical development

Labeling Operations Manager Associate

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMexicoNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree is required; a science or life sciences-related field is preferred.
  • Zero to two years of practical experience.
  • Complete fluency in English.
  • Strong logical, analytical, and writing ability.
  • High attention to detail.
  • Excellent computer skills and proficiency with Microsoft Word and similar applications.
  • Demonstrated project management skills and ability to assess and manage project timelines.
  • Ability to multitask, prioritize, and manage multiple projects.
  • Ability to identify and resolve problems proactively.
  • Appropriate decision-making, including escalating issues to the Global Labeling Lead and other appropriate stakeholders.
  • Ability to liaise with stakeholders using effective communication.
  • Ability to apply labeling regulatory guidance on formatting requirements.
  • Ability to consolidate comments from multiple sources, such as emails and meeting minutes.
  • Knowledge of labeling guidance and policies related to technical and formatting requirements, such as the QRD template and PLR format.
  • Ability to prepare submission-ready documents.

Responsibilities

  • Support the review and delivery of labeling documents and associated Patient Labeling Documents for non-complex products and projects.
  • Prepare comparison tables for labeling team discussions.
  • Generate clean and marked PDF and Microsoft Word renditions, and bookmark renditions as appropriate.
  • Facilitate document management workflows through the appropriate document management system.
  • Finalize documents after quality control.
  • Notify internal stakeholders when labeling documents are available.
  • Ensure compliance with company submission standards, policies, procedures, applicable standard operating procedures, and associated documents.
  • Consolidate comments from labeling reviewers and regulatory authorities.
  • Edit and format labeling documents and ensure compliance with the appropriate template, such as QRD or PLR.
  • Update and maintain the CDS log.
  • Set targets for review and approval timelines, follow up with Labeling Team members, and ensure deadlines are met.
  • Track labeling projects through defined procedures and use systems optimally.
  • Provide shadowing opportunities to Trainee LOMs.

About the Company

ClinChoice

Global CRO providing full-service clinical development

ClinChoice is a global contract research organization (CRO) that provides outsourced clinical development services across the full lifecycle for pharmaceutical, biotechnology, medical device, and consumer health customers. It delivers services such as clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance to support trials from early development through post-approval. The company differentiates itself with a large, global workforce—over 4,000 professionals in more than 30 countries—and growth through mergers and acquisitions, enabling multinational trial execution. Its goal is to help clients accelerate approvals and navigate complex regulatory environments by offering flexible project-based and FSP engagement models for end-to-end development and lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Whitemarsh Township, Pennsylvania
Founded
1995

Recently Posted Jobs

Explore more opportunities at ClinChoice

See more jobs