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Trainee Regulatory Associate

Navitas Life Sciences
Navitas Life Sciences
0-2 years
Not Disclosed
10 Sept. 18, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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
Location: Bogota, Colombia
Department: Regulatory Affairs
Reports To: Entry Level
Employment Type: Full-Time

Educational Qualification:

  • Bachelor’s degree in Pharmacy, Pharmaceutical Chemistry, or related life sciences field


Job Purpose:

Provide end-to-end publishing and regulatory support for initial and lifecycle maintenance of IND/NDA/MAA applications, ensuring high-quality submissions and compliance with global agency standards.


Key Responsibilities:

Regulatory Submission Support:

  • Manage end-to-end publishing support for initial IND/NDA/MAA applications and lifecycle maintenance globally.

  • Collaborate with cross-functional departments for planning, preparation, publishing, and quality control of submissions.

  • Support development of submission-ready documents, including formatting, hyperlinking, and processing MS Word and Adobe Acrobat documents.

  • Support eCTD, NeeS/eSub, and paper submissions for global agencies.

  • Troubleshoot document issues and identify gaps, addressing them with respective client stakeholders.

  • Manage technical aspects for assigned submissions and provide status updates.

  • Perform quality checks to ensure no unacceptable warnings or validation errors before submission.

Training & Knowledge Sharing:

  • Perform on-the-job training following the train-the-trainer model for beginners/fellow colleagues.

  • Provide QC feedback for continuous improvement.

  • Develop and maintain knowledge of established agency standards and regulatory submission procedures.

Regulatory Data Management:

  • Review and interpret data to determine system/tools requirements in line with SOPs and business processes.

  • Perform data entry and quality control tasks associated with regulatory systems.

  • Review new certificate requests, enter data in SharePoint, and follow up on cases to completion.

  • Identify issues, provide solutions, and perform retrospective remediation tasks.

  • Support global/local team members with data management workload as needed.

Coordination & Communication:

  • Coordinate ancillary requests and liaise with suppliers, in-country offices, manufacturing sites, or legalization teams to obtain required documents/samples.

  • Ensure timely delivery of required documents to clients for submissions.

  • Attend operational meetings and provide proactive support to the Regulatory team.

  • Project manage multiple requests simultaneously, ensuring deadlines and next action dates are maintained.

  • Escalate to point of contact when timelines may not be met.


Required Skills & Competencies:

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

  • Strong attention to detail, accuracy, and ability to manage multiple tasks.

  • Effective communication and collaboration skills.

  • Ability to learn quickly, follow SOPs, and maintain compliance standards.