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Regional Medical Advisor

0-2 years
Not Disclosed
10 Sept. 16, 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

Job Responsibilities

Medical & Scientific Expertise

  • Develop and maintain in-depth knowledge of assigned product(s) and therapeutic area(s) through participation in internal trainings, congresses, seminars, and independent literature review.

  • Provide expert medical/scientific advice on assigned products and therapeutic areas, including responding to requests for scientific/technical information.

  • Contribute to the development and ensure accuracy of medical core dossiers (e.g., medical information packs, clinical expert reviews).

Stakeholder Engagement & Scientific Communication

  • Establish and maintain strong professional relationships with key opinion leaders, academic centers, and external experts.

  • Participate in scientific congresses, advisory boards, round-table meetings, and discussion forums.

  • Deliver scientific presentations and medical education programs to healthcare professionals (individually or in groups).

  • Review literature and scientific society outputs, preparing summaries of key developments and trends relevant to the company.

Training & Knowledge Sharing

  • Design and deliver training sessions to sales forces and other departments.

  • Develop and update training materials to ensure medical and scientific accuracy.

Clinical Research Activities

  • Design and implement clinical research projects (e.g., Phase IV, post-marketing activities, registries, epidemiological surveys, PMOS studies) within defined standards and budgets.

  • Oversee review, approval, and conduct of Investigator-Initiated Studies (IIS).

  • Support the Clinical Research Department with study protocol reviews, investigator/site identification, and feasibility assessments.

Promotional & Commercial Support

  • Review and prepare promotional materials, ensuring scientific accuracy and compliance with Abbott policies and regulations.

  • Provide medical/scientific input into marketing strategies and commercial initiatives.

  • Monitor competitor activities (e.g., product strategies, studies, commercial positioning) and communicate insights internally.

Compliance & Governance

  • Ensure compliance with all applicable national laws, regulations, industry codes, Abbott policies, and ethical standards.


Technical Competencies

  • Management Skills

  • Communication Skills

  • Compliance & Process Improvement

  • Problem-Solving & Conflict Resolution

  • Priority Setting