Instagram
youtube
Facebook

Senior Medical Advisor

2+ years
Not Disclosed
10 March 4, 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

Senior Medical Advisor

Location: Mumbai, India
Category: Medical and Clinical Affairs

Job Description

Key Responsibilities:

  • Develop and maintain in-depth knowledge of assigned product(s) and therapeutic area(s) through internal training, congresses, seminars, and literature review.
  • Provide expert medical and scientific advice on assigned products, including responding to medical inquiries and ensuring scientific accuracy of core dossiers (e.g., medical information packs, clinical expert reviews).
  • Build and maintain credible relationships with key opinion leaders (KOLs), academic centers, and medical societies through congress participation, advisory boards, and round-table meetings.
  • Deliver scientific presentations and medical education programs to healthcare professionals (HCPs) in various formats (meetings, clinical sessions, etc.).
  • Analyze and summarize scientific literature and conference findings for internal teams, highlighting key insights on diagnosis, monitoring, and treatments in relevant therapeutic areas.
  • Provide training to sales teams and internal departments, ensuring the development and continuous update of training materials.

Clinical Research Activities:

  • Design and implement clinical research projects, including Phase IV studies, post-marketing surveillance, and epidemiological surveys, ensuring adherence to defined budgets and standards.
  • Oversee review, approval, and execution of Investigator-Initiated Studies (IIS).
  • Support clinical study management, including protocol review, investigator/site selection, and feasibility assessments in collaboration with the Clinical Research Department.

Medical and Commercial Strategy:

  • Review and approve promotional materials, ensuring scientific accuracy and compliance with company policies and regulations.
  • Contribute medical/scientific insights into marketing strategies and commercial initiatives.
  • Monitor competitive intelligence, tracking product strategies, clinical studies, and commercial positioning, and communicate insights within the organization.

Compliance & Process Improvement:

  • Ensure strict adherence to national regulations, industry guidelines, and internal Abbott policies.
  • Uphold best practices in compliance, communication, and process efficiency.

Technical Competencies:

  • Strong management and leadership skills
  • Excellent communication and presentation abilities
  • Deep understanding of compliance and process improvements
  • Effective problem-solving and conflict-resolution skills
  • Ability to prioritize tasks and manage multiple projects simultaneously