AstraZeneca is inviting applications for the position of Analyst – Medical Information Analyst in Bangalore, India. The role focuses on scientific content creation, medical information responses, evidence synthesis, medical literature research, and regulatory compliance for products marketed in the United States.
Candidates with an advanced scientific qualification or equivalent experience and a background in medical information, scientific communications, or related pharmaceutical and healthcare roles can apply through the official AstraZeneca careers portal.
Job Details
| Particulars | Details |
|---|---|
| Company | AstraZeneca |
| Job Title | Analyst – Medical Information Analyst |
| Location | Bangalore, India |
| Job Type | Full-time |
| Job Requisition ID | R-259295 |
| Job Grade | GCL: C3 |
| Date Posted | October 22, 2026 |
| Closing Date | October 24, 2026 |
About AstraZeneca
AstraZeneca is a global biopharmaceutical company focused on delivering medicines to patients. The Medical Information Analyst role supports healthcare professionals by providing accurate, timely, scientifically balanced, and compliant medical information about products marketed in the United States.
Positions Available
- Analyst – Medical Information Analyst
Job Responsibilities
The selected candidate will be responsible for:
- Developing, reviewing, updating, and maintaining medical information content, including US standard responses and localized scientific communication materials.
- Responding to medical information requests for US products with accurate, scientifically balanced, and timely information.
- Conducting literature searches and preparing customized responses to complex medical inquiries.
- Using medical information and content management systems to manage content creation, reviews, tracking, and reporting.
- Evaluating scientific evidence and ensuring appropriate citations and copyright compliance.
- Performing medical accuracy checks, quality assurance, editorial reviews, and promotional reviews.
- Building therapeutic area knowledge to develop relevant, customer-focused scientific content.
- Collaborating with scientific, medical, regulatory, and commercial teams.
- Managing projects and workstreams, prioritizing tasks, and addressing potential risks.
- Supporting digital innovation and adopting technologies, including AI, to improve content quality, response accuracy, and efficiency.
Eligibility and Qualifications
Candidates should meet the following requirements:
- An advanced scientific degree or equivalent experience; PharmD is preferred.
- MD, PhD, or an equivalent qualification is also mentioned.
- Demonstrated experience in medical information, scientific communications, or related roles within the pharmaceutical, biotechnology, or healthcare industry.
- Knowledge of clinical and healthcare systems.
- Ability to apply local regulatory, legal, and compliance requirements to Medical Affairs activities and drug information delivery.
Required Skills
- Excellent written and verbal communication skills.
- Scientific and medical writing, communication, and content creation, including slide decks.
- Ability to translate complex scientific information into clear, accurate messages for diverse audiences.
- Strong scientific research, literature evaluation, and evidence synthesis skills.
- Strategic problem-solving, project management, and organizational abilities.
- Ability to collaborate across teams and functions.
- Proficiency in using technology and digital platforms.
- Awareness of cultural differences and adaptability to change.
Desirable Skills
- Experience in digital content development or digital content strategy.
- Experience mentoring and coaching team members for senior roles.
- Familiarity with medical information and content management systems, including GMIP Inquiry, Vault MedComms, PromoMats, and AIMI.
- Familiarity with US medical information processes.
Work Model
The position follows an in-person working expectation of an average minimum of three days per week in the office, with flexibility considered within the company’s working arrangements.
