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Senior Associate, Global Submission Management - Americas

4-6 years
Not Disclosed
10 April 9, 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: Senior Associate, Global Submission Management - Americas
 Location: India – Hyderabad
 Work Location Type: On Site
 Job ID: R-206628
 Date Posted: April 3, 2025
 Category: Regulatory


Job Summary

The Senior Associate, Global Submission Management – Americas is responsible for the compliant flow of regulatory information, collaborating with internal teams, external partners, and regulatory authorities across North America. The role involves planning and managing regulatory submission components and dossiers, with a focus on technical compliance and operational excellence.


Roles & Responsibilities

  • Lead/support Clinical Trial and Marketing Application submissions.

  • Manage Global/Submission Content Plans.

  • Participate in system updates and ongoing system validations.

  • Serve as the point of contact for regulatory submission delivery and archiving (Veeva Vault RIM).

  • Stay updated on internal/external regulatory guidance.

  • Represent departmental expertise in global/regional projects.

  • Ensure regulatory documentation processes are followed from a publishing perspective.

  • Contribute to global health authority communication strategies.

  • Lead and manage process improvements.

  • Work across departments to ensure timely submission execution.


Required Knowledge and Skills

  • Advanced project management and technical skills.

  • Experience in leading cross-functional teams.

  • Strong knowledge of global regulatory submissions in eCTD, NeeS, and paper formats.

  • Expertise in Veeva Vault RIM and submission content management.

  • Familiarity with eCTD software (preferably Lorenz docuBridge Explorer).

  • Knowledge of regional submission requirements (Global, US, Canada, South America).


Preferred Knowledge and Skills

  • Deep understanding of regulatory guidance for Clinical Trials and Marketing Applications.

  • Strong collaboration across regulatory-related functions (Clinical, CMC, Nonclinical, Safety, etc.).

  • Advanced use of dashboards and submission tracking tools.


Education and Experience Requirements

Minimum (any one of the following):

  • Master’s degree with 3–4 years of relevant experience

  • Bachelor’s degree with 4–6 years of relevant experience

  • Associate’s degree with 6–8 years of relevant experience

  • High school diploma / GED with 8+ years of relevant experience

Preferred:

  • Hands-on experience with submission processes for the US, Canada, and South America.