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Medical Information Specialist

Propharma
Propharma
1-3 years
Not Disclosed
Remote
10 March 2, 2026
Job Description
Job Type: Full Time Hybrid Remote 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

Medical Information Specialist (MIS) – Drug Safety & Scientific Communications

Location: India (Remote / Hybrid as per business requirements)
Employment Type: Full-Time
Job Requisition ID: JR 9028
Department: Medical Information Contact Center

About the Organization

ProPharma is a global life sciences consulting organization supporting biotechnology, pharmaceutical, and medical device companies across the complete product lifecycle. Through its advise–build–operate model, ProPharma delivers expertise in regulatory sciences, clinical research, pharmacovigilance, medical information, quality & compliance, and R&D technology. With over 20 years of industry leadership, the organization helps accelerate innovation while ensuring regulatory compliance and patient safety.

About the Role

ThePharmaDaily.com invites applications for the position of Medical Information Specialist (MIS) in India. This full-time role is part of the Medical Information Contact Center and plays a critical role in delivering accurate, compliant, and timely medical and safety information to healthcare professionals (HCPs), consumers, and external stakeholders.

The Medical Information Specialist ensures adherence to global regulations, industry standards, and internal Standard Operating Procedures (SOPs) while managing adverse event documentation, product complaints, and scientific inquiries.

Key Responsibilities

Medical Information Service Delivery

  • Respond to unsolicited medical and safety information requests received via telephone, email, website, fax, letter, or scientific meetings on behalf of pharmaceutical clients

  • Provide labeled and unlabeled product information in compliance with regulatory requirements and internal policies

  • Accurately identify, document, and report adverse events, pregnancy reports, special situation events, and product quality complaints in accordance with global regulations and SOPs

  • Ensure timely completion of tasks as per agreed timelines in SOPs and Working Practices (WPs)

  • Formulate scientifically accurate responses using approved labeling, standard response documents, and published literature

  • Assist in drafting customized medical information responses

  • Log all inquiries accurately and comprehensively within inquiry handling systems

Quality Assurance & Compliance

  • Perform quality checks on adverse event documentation, product complaints, and inquiry records

  • Maintain strict adherence to data privacy and confidentiality regulations

  • Comply with company health and safety policies

  • Provide after-hours coverage on a rotational basis as per business needs

  • Support additional activities as delegated by management

Eligibility & Qualifications

  • Degree in Life Sciences OR Nursing (RN/BS/BA/MS) OR Pharmacy (B.Pharm/M.Pharm/PharmD)

  • Strong working knowledge of medical terminology, pharmacology, pathophysiology, and industry regulations

  • Excellent verbal and written communication skills with professional telephone etiquette

  • Ability to draft scientifically accurate and grammatically correct responses in English

  • High proficiency in Microsoft Office applications and Adobe Acrobat

  • Experience with document management systems and inquiry handling databases preferred

Experience Required

  • 1–3 years of experience in Medical Information, Pharmacovigilance, Drug Safety, or related life sciences roles preferred

  • Fresh graduates with strong scientific writing skills and relevant internship exposure may also be considered

Core Competencies

  • Strong analytical thinking and critical reasoning skills

  • Ability to multitask while maintaining high accuracy under strict timelines

  • Effective stakeholder communication and customer service orientation

  • Independent problem-solving ability and proactive mindset

  • Strong organizational and prioritization skills

  • Ability to work independently and collaboratively in a team environment

Work Model

While remote working is supported, hybrid collaboration may be encouraged for candidates located within commuting distance of office locations, subject to managerial agreement.

Diversity & Inclusion Commitment

The organization fosters an inclusive work culture built on diversity, equity, and equal opportunity. All applications are reviewed by a dedicated recruitment team member, and every candidate receives a formal application outcome.

Application Process

Applications will be evaluated based on qualifications, communication proficiency, and relevant industry experience. Shortlisted candidates will be contacted for further assessment and interviews.

This role is ideal for professionals seeking to advance their career in Medical Information, scientific communications, regulatory-compliant customer engagement, and global drug safety operations within the pharmaceutical and biotechnology industry.