Job Title: Medical Information Writer
Company: ProPharma
Location: India
Job Type: Full-Time
Job ID: JR 9127
Experience Required: 0–2 Years (Fresh PharmD Graduates Eligible)
About ProPharma
ProPharma is a global consulting organization that supports pharmaceutical, biotechnology, and medical device companies across the entire product lifecycle. For more than 20 years, ProPharma has helped organizations advance scientific innovation by providing expertise in regulatory sciences, clinical research solutions, pharmacovigilance, medical information, quality and compliance, and research and development technology. Through its comprehensive advise-build-operate model, ProPharma delivers customized solutions that help partners accelerate drug development while maintaining regulatory compliance and patient safety.
Role Overview
The Medical Information Writer is responsible for developing scientifically accurate medical content used to respond to inquiries received by medical information teams. This includes preparing technical responses, medical information letters, and frequently asked questions (FAQs) based on scientific literature and approved product information. The role requires strong medical writing skills, the ability to analyze scientific data, and the capability to transform complex clinical information into clear and concise responses for healthcare professionals and internal stakeholders.
This position is ideal for PharmD graduates interested in pursuing a career in medical writing, medical communications, or pharmaceutical medical information services.
Key Responsibilities
Medical Information Content Development
Prepare technical responses, medical information letters, and frequently asked questions (FAQs) to address inquiries from healthcare professionals and internal stakeholders.
Develop new standard response documents and update existing medical information materials as required.
Translate complex scientific and clinical information into clear, accurate, and concise written responses.
Scientific Literature Research
Conduct comprehensive literature searches using databases such as MEDLINE and other scientific resources.
Analyze and extract relevant data from clinical studies, medical publications, and regulatory documents to support medical responses.
Summarize scientific evidence to create structured and evidence-based documentation.
Document Review and Maintenance
Review and update existing medical information documents to ensure accuracy and relevance.
Incorporate newly published scientific data into existing response documents while maintaining readability and scientific integrity.
Ensure consistency and compliance with company standards and client-specific working practices.
Quality Assurance and Compliance
Perform quality checks on personal work and support review of simple documents within the team under supervision.
Ensure all documentation complies with internal Standard Operating Procedures (SOPs) and regulatory requirements.
Maintain high standards of scientific accuracy and clarity in all written materials.
Regulatory and Ethical Compliance
Maintain awareness of legal and professional guidelines governing the provision of medical information within the pharmaceutical industry.
Ensure compliance with data privacy regulations and confidentiality requirements for client and company information.
Adhere to internal policies related to documentation, information security, and professional conduct.
Educational Qualifications
Doctor of Pharmacy (PharmD) degree is required.
Experience Requirements
0–2 years of experience in medical writing, medical information services, pharmacovigilance, or related pharmaceutical roles.
Fresh PharmD graduates with strong medical writing and research skills are encouraged to apply.
Required Skills and Competencies
Excellent scientific and medical writing skills.
Strong written communication and documentation abilities.
High attention to detail and accuracy in technical content.
Ability to interpret and summarize complex clinical and scientific information.
Strong organizational and time management skills.
Ability to work effectively in a collaborative team environment.
Technical Skills
Proficiency in Microsoft Office applications including Word, Excel, and PowerPoint.
Familiarity with medical literature databases such as MEDLINE or PubMed is preferred.
Work Environment
ProPharma supports flexible working arrangements, including remote and hybrid work models depending on project and team requirements. The organization encourages collaboration while providing flexibility to support productivity and work-life balance.
Job Location
India.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Anakapali | Anantapur | Bhimavaram | Chittoor | Guntur | Gurgaon | Kakinada | Mangalagiri | Nellore | Pydibimavaram | Tirupathi | Vijayawada | Visakhapatnam |Tamil Nadu :
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Dehradun | Halifax | Nainital | Rishikesh | Roorkee |Delhi :
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Hajipur | Patna |Kerala :
Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Rangpo |India :
Siliguri |Illinois :
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Germany | GErmany |Lower Saxony :
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Dún Laoghaire |Galway :
Galway |County Dublin :
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China | Quarry Bay |Liaoning :
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Queensland |Melbourne :
South Yarra |United Kingdom :
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Sheffield |Oxfordshire :
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Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
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Argentina | Peru |Brazil :
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Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
Vienna |Catalonia :
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Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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