Medical Information Manager

Latinum HR Solutions; Bengaluru; On-site; INR 900,000 - 1,500,000; Full time

Job summary

Latinum HR Solutions is hiring a Medical Information Manager to support global medical information activities. You will develop SRDs, FAQs and evidence-based responses while ensuring scientific accuracy and regulatory compliance.

You will conduct literature reviews, collaborate with Medical Affairs and Regulatory teams, and maintain medical content libraries with the latest clinical and safety data. This role requires 3–5 years in life sciences and a strong writing background.

Qualifications

• SRDs, FAQs and customized medical enquiry responses are developed.
• Literature reviews conducted to synthesize evidence-based medical content.
• Responses are scientifically accurate, non-promotional, and regulatory compliant.
• Collaborations with Medical Affairs, Clinical Development and Regulatory Affairs.
• Content libraries updated with new clinical and safety data.

Responsibilities

• Develop and author Standard Response Documents (SRDs) and FAQs.
• Create customized medical enquiry responses with evidence synthesis.
• Ensure responses are accurate, non-promotional and regulatory compliant.
• Collaborate with Medical Affairs, Clinical Development, Regulatory Affairs.
• Maintain and update medical content libraries with new data.

Skills

Scientific Writing

Literature Review

Medical Information Writing

Regulatory Compliance

Cross-functional Collaboration

Education

BSc Life Sciences

Advanced degree (PharmD/PhD/MD)

Tools

Veeva MedCom

CARA

IRMS

EndNote

Job description

We're Hiring | Medical Information Manager | Life Sciences

Are you passionate about scientific writing and medical communications We're looking for an experienced Medical Information Manager to join a dynamic team supporting global medical information activities.

Eligibility Criteria

• Locations: Hyderabad, Mumbai, Bangalore, Noida
• Experience: 3-5 Years
• Domain : Life Sciences
• Budget : Upto 15 LPA (Depending on Exp)
• Minimum 2 years of experience in authoring/developing medical enquiry responses

Role Overview

• Develop and author Standard Response Documents (SRDs), FAQs, and customized medical enquiry responses.
• Conduct scientific literature reviews and synthesize evidence-based medical content.
• Ensure responses are scientifically accurate, non-promotional, and compliant with regulatory guidelines.
• Collaborate with cross-functional teams including Medical Affairs, Clinical Development, and Regulatory Affairs.
• Maintain and update medical content libraries based on new clinical and safety data.

Key Skills

• Scientific & Medical Writing
• Literature Search & Critical Appraisal
• Medical Information Response Development
• Medical Affairs & Regulatory Compliance
• Reference Management (EndNote/Reference Manager)
• v Experience with Medical Information Systems (e.g., Veeva MedCom, CARA, IRMS)

Education

• Bachelor's degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related healthcare field
• (Advanced degree such as PharmD, PhD, or MD is an advantage.)