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Global Medical Development Manager

3-5 years
Not Disclosed
10 Feb. 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Global Medical Development Manager

Job ID: 388966BR
Date Posted: 07/01/2025
Location: India


Job Description

Your Key Responsibilities:

Your responsibilities include, but are not limited to:

  • Receive, triage, coordinate, and respond to inquiries from external and internal customers via Medical Information communication channels (e.g., call center, email, fax).

  • Provide medical and technical information to healthcare professionals, consumers, and internal staff across a wide range of products and therapeutic areas.

  • Deliver timely, accurate, balanced, and up-to-date scientific responses based on Global Guidance Documents (GGDs).

  • If the response is not available in GGDs, search, evaluate, and summarize the literature using critical judgment and professional/scientific expertise.

  • Prepare accurate announcements to disseminate official drug information for compendium entries (e.g., MIMs, BNF, eMC) to meet patient, medical, and legal requirements.

  • For assigned products, create and maintain scientifically balanced, product-specific medical information standard response documents in the Medical Information database.

  • Assist with compliance and safety teams for documenting and reporting adverse drug reactions as well as technical/product complaints requiring specialist input.

  • Collect, synthesize, and communicate insights relevant to the brand or market issues (e.g., quality, supply, enquiry patterns) during scientific interactions.

  • Report technical complaints, adverse events, and special case scenarios related to Novartis products within 24 hours of receipt.

  • Manage the distribution of marketing samples (where applicable).


What You’ll Bring to the Role:

Essential Requirements:

  • Project Management.

  • Operations Management and Execution.

  • Collaborating across boundaries.

Skills:

  • Medical Governance.

  • Medical Education and Scientific Engagement.

  • Third-Party Sponsored Trials.

  • Medical Science and Disease Area Knowledge.

  • STEAM - Applied Science, Technology, Engineering, Arts, Math.

  • Preclinical Safety.

  • Medical Information.

  • Medical Safety.

  • Publication Strategy, Planning, and Tactics.

  • Pharmacology/Toxicology.