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Medical Information Specialist

0-2 years
Not Disclosed
10 March 28, 2025
Job Description
Job Type: Full Time Education: PharmD/PhD/MSc/B.Pharm/M.Pharm 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

Medical Information Specialist
Location: Pune, Maharashtra, India
Job Type: Full-time
Department: Customer Service
Job Family: Medical & Regulatory Affairs

Company Description:
EVERSANA is recognized as a Great Place to Work globally. With a team of over 7,000 employees, we are dedicated to delivering next-generation commercialization services to the life sciences industry. Our services support over 650 clients, ranging from biotech start-ups to established pharmaceutical companies, helping bring innovative therapies to market and improving patient lives.

Job Description
The Position:
The Medical Information Specialist plays a key role in ensuring the safe and effective use of pharmaceutical products by providing scientifically balanced, evidence-based, non-promotional information in response to inquiries from healthcare professionals, patients, caregivers, and payers. This position supports multiple clients, products, and therapeutic areas while maintaining industry-leading service standards.

Essential Duties and Responsibilities:

  • Respond to medical information inquiries from healthcare professionals, consumers, and payers.

  • Research and critically evaluate medical literature to create accurate responses to inquiries.

  • Develop adverse event and product complaint narratives during intake.

  • Manage requests through various channels (phone, email, CRM, chat, etc.).

  • Identify and report adverse events and product complaints following FDA regulations and EVERSANA-MICC procedures.

  • Coordinate processes related to product quality complaints, working with departments such as Quality Assurance and Regulatory Affairs.

  • Maintain knowledge of products, therapeutic areas, and client-specific requirements.

  • Ensure high-quality documentation and excellent customer service.

  • Demonstrate commitment to diversity, equity, and inclusion through continuous learning and modeling inclusive behaviors.

Minimum Knowledge, Skills, and Abilities:

  • Strong clinical background with excellent verbal and written communication skills.

  • Ability to document effectively and handle complex medical inquiries.

  • Proficiency in English (spoken and written).

Qualifications:

  • Education: Pharm.D, M.Sc., B.Pharm, M.Pharm, or any other Life Sciences degree.

  • Strong clinical knowledge with prior experience in medical information, pharmacovigilance, or regulatory affairs preferred.

Additional Information:
EVERSANA is an Equal Opportunity Employer committed to fostering diversity, equity, and inclusion. All information will be kept confidential in accordance with EEO guidelines.

Recruitment Notice:
Beware of recruitment fraud misrepresenting EVERSANA. We do not require payment or personal information during the employment process.

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