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Medical Information Specialist

Propharma
0-3 years
INR 4 LPA – 7 LPA
PAN-India, India
1 June 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: CPT, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, Medical Billing, Medical Coding

Medical Information Specialist

Location: India
Employment Type: Full-Time

About ProPharma

For over 25 years, ProPharma has helped improve patient health and wellness by providing expert consulting and operational support to pharmaceutical, biotechnology, and medical device companies. Through its Advise-Build-Operate model, ProPharma supports clients throughout the entire product lifecycle, offering expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology.


Role Summary

The Medical Information Specialist is responsible for delivering high-quality medical information services by responding to inquiries from healthcare professionals, patients, and consumers. The role involves providing accurate medical and safety information, documenting adverse events, maintaining regulatory compliance, and supporting the safe and effective use of healthcare products.


Key Responsibilities

Medical Information Services

  • Respond to medical and safety-related inquiries received from healthcare professionals, patients, and consumers via phone, email, and web-based platforms.

  • Provide accurate and balanced responses using approved product information, scientific literature, and internal resources.

  • Prepare customized medical responses when required using client-approved references and supporting data.

  • Ensure all responses are delivered in a professional, compliant, and timely manner.

Safety Reporting & Documentation

  • Identify, document, and report:

    • Adverse Events (AEs)

    • Product Complaints

    • Other safety-related information

  • Ensure compliance with applicable regulatory requirements and company procedures.

  • Accurately log all inquiries and safety information into internal systems within required timelines.

Quality & Compliance

  • Perform quality checks on medical inquiries and safety reports.

  • Maintain high standards of documentation accuracy and completeness.

  • Follow internal SOPs, regulatory requirements, and client-specific processes.

Team Support & Process Improvement

  • Provide informal guidance and mentorship to new team members as experience develops.

  • Contribute ideas for process improvements and operational efficiencies.

  • Support updates to internal procedures and best practices.

Additional Responsibilities

  • Participate in after-hours support coverage on a rotational basis, subject to business requirements.

  • Undertake additional duties as assigned by management.


Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Nursing

    • Medicine

    • Other Healthcare-Related Disciplines


Required Skills & Competencies

  • Excellent verbal and written communication skills.

  • Strong customer service and interpersonal skills.

  • High attention to detail and commitment to accuracy.

  • Strong scientific and analytical thinking abilities.

  • Ability to communicate complex medical information clearly and effectively.

  • Interest in:

    • Drug Safety

    • Medical Information

    • Pharmacovigilance

    • Regulatory Affairs

  • Proactive and self-motivated approach to learning and development.

  • Strong organizational and time-management skills.

  • Ability to work independently and collaboratively within a team environment.


Career Growth & Benefits

Career Development

  • Structured career progression opportunities.

  • Internal promotion-focused culture, with leadership roles frequently filled from within.

  • Comprehensive onboarding and continuous professional development programs.

  • Access to leadership, management, and industry-specific training.

Work Environment

  • Flexible and remote working opportunities.

  • Collaborative and multicultural global team environment.

  • Exposure to leading pharmaceutical, biotechnology, and medical device organizations.

Employee Benefits

  • Performance-related pay and annual bonus opportunities.

  • Health and wellness support programs.

  • Retirement and pension-related benefits.

  • Enhanced family leave policies.

  • Additional employee wellbeing initiatives and benefits.


Key Skills

  • Medical Information

  • Pharmacovigilance

  • Adverse Event Reporting

  • Drug Safety

  • Scientific Literature Review

  • Medical Writing

  • Regulatory Compliance

  • Healthcare Communication

  • Product Safety

  • Customer Support

  • Quality Assurance

  • Documentation Management