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Trainee Regulatory Associate

Navitas Life Sciences
Navitas Life Sciences
0-2 years
Not Disclosed
10 May 28, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Trainee Regulatory Associate


Job Overview

We are currently seeking a Trainee Regulatory Associate to join our growing team in Colombia. This entry-level position supports regulatory publishing, data management, and coordination of regulatory activities in compliance with global health authority requirements.


Key Responsibilities

Regulatory Publishing & Submissions

  • Support end-to-end publishing for IND/NDA/MAA applications and life cycle maintenance globally

  • Collaborate with cross-functional teams for planning, formatting, hyperlinking, and quality control checks

  • Format documents using MS Word and Adobe Acrobat for submission-readiness

  • Ensure outputs meet eCTD, NeES/eSub, and paper submission standards

  • Troubleshoot formatting and document issues; liaise with client stakeholders to resolve

  • Perform quality checks ensuring no validation errors prior to submission

  • Maintain up-to-date knowledge of global agency standards and submission requirements

Regulatory Data Management

  • Review and interpret data to establish appropriate systems/tools in line with SOPs

  • Perform data entry and quality control in regulatory systems

  • Review new certificate requests, manage SharePoint data, and track case progress

  • Coordinate and manage centralized data support and retrospective remediation tasks

Operational Support

  • Manage ancillary requests via client systems and coordinate with suppliers/in-country offices

  • Ensure complete delivery of documents for regulatory submissions

  • Attend operational meetings and support the Product Licensing Support Team

  • Manage multiple concurrent requests and track deadlines and next actions using system reports

  • Escalate issues when timeline risks arise

Training & Team Collaboration

  • Participate in on-the-job training using a train-the-trainer approach

  • Provide QC feedback to improve team processes

  • Support global/local teams with workload balancing across regulatory tasks


Desirable Skills and Experience

  • Proficient in MS Word, Excel, PowerPoint, Access, and Adobe Professional

  • Strong organizational and time-management skills

  • Detail-oriented with a quality-focused mindset

  • Ability to multitask and meet deadlines

  • Strong communication and coordination skills

  • Quick learner, self-motivated, and team-oriented