Regional Medical Advisor (CVRM) – Mumbai
Location: Mumbai, Maharashtra, India
Job ID: R-238420
Date Posted: 30/10/2025
Closing Date: 19/11/2025
Company: AstraZeneca
1. About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company specializing in the discovery, development, and commercialization of prescription medicines for serious diseases. The organization prioritizes innovation, scientific excellence, and patient outcomes.
2. Role Summary
The Regional Medical Advisor (RMA) is a field-based scientific expert in the assigned therapeutic area (CVRM). The role supports the execution of Medical Affairs Plans for pre-launch or newly launched products and shapes clinical practice through scientific engagements, partnerships, and insight generation.
3. Key Responsibilities
A. Scientific Expertise
Maintain expertise in disease management, AstraZeneca products, emerging therapies, and competitive landscape.
Lead and contribute to the Field Medical Strategic Plan (FMSP).
Serve as a scientific resource for internal and external stakeholders.
Support internal teams through training and mentoring.
B. Scientific Exchange
Conduct peer-to-peer scientific dialogue with HCPs and other stakeholders.
Provide balanced scientific information in response to unsolicited inquiries.
Deliver clinical/scientific presentations to internal and external audiences.
Build relationships with key experts and thought leaders.
Facilitate scientific events:
MSL meetings
Symposiums
Advisory boards
Expert panels
Standalone non-promotional events
“Meet the Professor” sessions
Collaborate with KEEs on study proposals (ESR/local studies).
C. Customer Insights
Gather, analyze, and communicate insights from scientific and clinical environments.
Provide actionable insights to shape medical and product strategies.
Identify gaps in the patient journey and inform strategy development.
D. Strategic Relationships
Build and maintain relationships with HCPs, institutions, government bodies, PAGs, payers, and innovative ecosystem partners.
Identify investigators for clinical and post-marketing studies.
Support data generation and investigator-sponsored studies.
Build strategic, sustainable, and scalable partnerships to enhance patient access.
E. Other Key Responsibilities
Utilize digital tools and innovative technologies for scientific exchange.
Strong understanding of:
Pharmacovigilance (PV)
GxP principles
Good Clinical Practice (GCP)
Clinical study types
AE reporting requirements
Provide training on ethical interactions, compliance standards, and local regulations.
Ensure adherence to internal SOPs, field medical standards, and local regulatory guidelines.
4. Required Qualifications
Essential
Scientific degree or master's degree in a relevant scientific field.
Excellent communication and interpersonal skills.
Strong project management and presentation capabilities.
Analytical and conceptual thinking abilities.
Ability to engage across multiple communication channels.
Desirable
Doctoral degree (MD, PhD, PharmD).
Experience in pharmaceutical industry, regulatory environment, or clinical research.
Experience in drug development, basic research, and interactions with KEEs.
5. Key Working Relationships
Internal
Medical Affairs
MedEx
Regulatory Affairs
Pharmacovigilance
Medical Information
Commercial (Marketing & Sales)
Compliance team
Diagnostics, SMM, and related functions
External
Healthcare professionals
Hospital/Healthcare institutions
Policy makers
Research institutions
PAGs
Startups and innovators
Service providers
6. Why Join AstraZeneca?
Highly collaborative, inclusive, and growth-driven workplace.
Opportunities to innovate and impact patient care.
Emphasis on diversity, lifelong learning, and professional development.
7. Next Steps
Interested candidates should apply before 19 November 2025.
For more information, reach out to the provided contact person.
8. Social Media Links
LinkedIn – AstraZeneca
Facebook – AstraZeneca Careers
Instagram – @astrazeneca_careers
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