Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
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