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Regional Medical Advisor (Cvrm) – Bangalore

Astrazeneca
AstraZeneca
5-7 years
preferred by company
10 Jan. 21, 2026
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 Title: Regional Medical Advisor (CVRM)
Job Requisition ID: R-243622
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time | Field-Based
Date Posted: 14 January 2026
Application Closing Date: 23 January 2026


Job Overview

AstraZeneca is seeking a Regional Medical Advisor (CVRM) to join its Medical Affairs team in Bengaluru, India. This field-based role focuses on Cardiovascular, Renal, and Metabolic (CVRM) therapeutic areas and plays a pivotal role in executing medical strategies for pre-launch and newly launched products.

As a Regional Medical Advisor, you will act as a trusted scientific partner to healthcare professionals and healthcare ecosystem stakeholders, driving evidence-based clinical practice, scientific exchange, and improved patient outcomes through high-quality medical engagements.


Key Responsibilities

Scientific Expertise & Medical Strategy

  • Maintain deep scientific and clinical expertise in CVRM disease areas, AstraZeneca products, emerging therapies, and the competitive landscape.

  • Contribute to and lead components of the Field Medical Strategic Plan (FMSP) for the assigned therapeutic area.

  • Act as a subject matter expert for internal stakeholders across Medical Affairs, Regulatory Affairs, Pharmacovigilance, and Commercial teams.

  • Support the development and delivery of therapeutic area training and mentoring initiatives.

Scientific Exchange & Stakeholder Engagement

  • Engage in high-quality, peer-to-peer scientific dialogue with healthcare professionals, KEEs, and other relevant stakeholders.

  • Deliver balanced, non-promotional scientific information in response to unsolicited medical inquiries.

  • Organize and lead scientific events including advisory boards, MSL meetings, symposia, expert panels, and “Meet the Professor” sessions.

  • Present scientific and clinical data at internal and external meetings aligned with medical communication strategies.

Evidence Generation & Insights

  • Collaborate with KEEs on investigator-sponsored research (ISR/ESR), local studies, and relevant publications.

  • Identify, analyze, and communicate actionable medical and scientific insights to internal stakeholders to inform product and medical strategies.

  • Partner with traditional and non-traditional stakeholders to identify gaps in patient journeys and healthcare delivery.

Strategic Partnerships & Compliance

  • Build and sustain peer-level relationships with medical experts, research institutions, government bodies, and healthcare ecosystem partners.

  • Support identification and engagement of investigators for pre-clinical, clinical, and post-marketing studies.

  • Ensure strict adherence to pharmacovigilance, GxP, ethical interaction policies, and local/global compliance standards.

  • Leverage digital tools, innovation, and technology to enhance scientific exchange and patient-centric solutions.


Required Qualifications & Experience

Education:

  • Master’s degree in a scientific discipline (Life Sciences, Pharmacy, Medicine, or related field).

Experience Required:

  • Minimum 5–7 years of experience in Medical Affairs, Medical Advisor, or MSL roles within the pharmaceutical or biopharmaceutical industry.

  • Demonstrated experience in therapeutic area engagement, preferably within Cardiovascular, Renal, or Metabolic (CVRM) diseases.

Core Skills:

  • Excellent written and verbal communication and presentation skills.

  • Strong project management and analytical capabilities.

  • Ability to engage effectively across multiple communication channels and stakeholder groups.

  • Solid understanding of pharmacovigilance, GxP, GCP, clinical studies, and adverse event reporting.


Preferred Qualifications

  • Doctoral degree such as MD, PhD, or PharmD.

  • Experience in clinical or pre-clinical research, regulatory environments, and investigator interactions.

  • Background in drug development, evidence generation, and scientific publications.


Key Skills (SEO Optimized)

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Why Join AstraZeneca

At AstraZeneca, you will be empowered to push the boundaries of science while working in an inclusive, collaborative environment. The organization is committed to lifelong learning, innovation, and improving patient outcomes worldwide through cutting-edge science and responsible medical leadership.


Apply now to advance your career in Medical Affairs and CVRM leadership.
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