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Medical Information Specialist

0-1 years
Not Disclosed
10 Dec. 17, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

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


Company Description:

At EVERSANA, we are proud to be certified as a Great Place to Work globally. We are driven by a vision to create a healthier world, supported by over 7,000 employees who are dedicated to delivering next-generation commercialization services to the life sciences industry. Serving more than 650 clients, including innovative biotech startups and established pharmaceutical companies, we help bring cutting-edge therapies to market and support the patients who depend on them. Join our team to make an impact and be part of a diverse, inclusive culture.


Job Description:

The Medical Information Specialist plays a key role in providing timely, scientifically balanced, and evidence-based information to healthcare professionals, patients, caregivers, and payers. This role involves responding to unsolicited requests for product information and handling adverse events and product complaints in a customer-centric manner. As a member of the Medical Information Contact Center (MICC) team, you will support multiple pharmaceutical clients and therapeutic areas, providing expert-level knowledge and services.

Key Responsibilities:

  • Respond to medical inquiries from healthcare professionals, consumers, and payers through various communication channels (phone, email, CRM, chat).
  • Research and critically evaluate medical literature to create accurate, evidence-based responses.
  • Handle adverse event and product complaint intake, generating reports in compliance with FDA regulations and EVERSANA-MICC SOPs.
  • Coordinate with relevant departments (e.g., Quality Assurance, Regulatory Affairs) to address product quality complaints.
  • Maintain knowledge of products, therapeutic areas, and client-specific requirements.
  • Ensure quality documentation and excellent customer service.
  • Demonstrate a commitment to diversity, equity, and inclusion through continuous development and inclusive behaviors.

Qualifications:

  • Education: Pharm.D, Master of Science (MSc), B.Pharm, M.Pharm, or any other Life Sciences degree.
  • Strong clinical background with excellent documentation, verbal, and written communication skills.
  • Fluent in English (spoken and written).

Preferred Qualifications:

  • Expertise in medical documentation, critical thinking, and analytical skills.
  • Knowledge of FDA post-marketing adverse event reporting and safety terminology.

Why EVERSANA?

At EVERSANA, we embrace diversity, equity, and inclusion as core values. We are an Equal Opportunity Employer and value the unique experiences, perspectives, and backgrounds of our employees. If you're passionate about improving patient lives and shaping the future of healthcare, EVERSANA is the place for you!