Senior Medical Writer

Galderma; India; Híbrido; INR 1 200 000 - 1 800 000; Tempo integral

Resumo da oferta

Galderma in India hybrid is seeking an experienced medical writer to translate complex evidence into clear, accurate content for healthcare professionals. The role demands strong biomedical science understanding, clinical research interpretation, and timely delivery of manuscripts, abstracts, posters and publications.

You will ensure compliance with ICMJE, GPP3, journal requirements, and privacy and disclosure standards while collaborating with cross-functional experts to meet deadlines across

Qualificações

• Minimum science degree or equivalent with 6+ years of scientific writing experience.
• Experience in biologics (dermatology preferred).
• Hands-on experience with MS Word, PowerPoint, Excel and related tools.
• Datavision and Veeva experience preferred.

Responsabilidades

• Lead planning, development, review, submission and delivery of manuscripts and related scientific materials.
• Evaluate data, identify key insights, and develop balanced scientific narratives.
• Maintain accuracy, consistency, referencing and quality control.
• Adapt scientific content for healthcare professionals with appropriate tone and detail.
• Apply EMA/FDA requirements and QRD standards, including SmPC guidelines and disclosure principles.
• Collaborate with cross-functional teams and manage multiple priorities in a fast-paced environment.
• Develop knowledge of evolving science and therapeutic areas; maintain project records and SOP compliance.

Conhecimentos

Medical writing

Scientific writing

Regulatory writing

Communication skills

Biomedical science

Formação académica

MSc/MPharm/PhD or equivalent

Ferramentas

MS Word

PowerPoint

Excel

Datavision

Veeva

Descrição da oferta de emprego

Department: GMA Excellence and Operations

Position Reports to: Head of MSH

Location: India Hybrid

Position summary

The ideal candidate is an experienced medical writer with an established track record combining scientific expertise with exceptional communication skills, translating complex evidence into clear, accurate and engaging content for healthcare professionals.

Strong understanding of biomedical science, clinical research and evidence interpretation. Ability to communicate complex scientific concepts accurately, concisely and accessibly. Track record of strong collaboration. Prioritization meeting critical deadlines with a growth mindset enabling learning across our respective therapeutic areas.

Role and Responsibilities

• Lead the planning, development, review, submission, and delivery of manuscripts, abstracts, posters, presentations, consensus papers, and related scientific materials.
• Skilled in evaluating data, identifying key insights and developing balanced scientific narratives.
• Meticulous approach to accuracy, consistency, referencing and quality control.
• Understands the information needs of healthcare professionals and adapts scientific content, tone and level of detail to support clear, relevant and credible manuscripts, posters, abstracts and other forms of medical publications.
• Demonstrates strong knowledge of and applies applicable medical writing, publication and research-reporting standards, including relevant European Medicines Agency (EMA) / US Food and Drug Administration(FDA) requirements and guidance, such as current product-information, Summary of Product Characteristics (SmPC) and Quality Review of Documents (QRD) standards.
• Is Familiar with ICMJE Recommendations, Good Publication Practice (GPP), relevant journal requirements, authorship and disclosure principles, demonstrate reference accuracy, copyright, data privacy and company review and approval processes is also required. Applies these requirements with scientific integrity, transparency and balanced, non-promotional communication for healthcare professionals.
• Works effectively with cross-functional experts and incorporates feedback constructively..
• Manages multiple priorities, meets deadlines and performs well in a fast-paced environment.
• Proactively develops knowledge of evolving science, therapeutic areas and communication practices.
• Maintains records for all assigned projects including archiving. SOP and training compliance.

Education and Work Experience

• Minimum science degree or equivalent - M.Sc./ M. Pharma B.Sc. Doctoral Degree or Qualification in Medical Sciences /equivalent with minimum of + 6 years scientific writing experience,
• Experience in working on biologics (ideally in dermatology) preferred
• Hands on experience working on MS Word, PowerPoint, Excel and other related tools
• Hands on experience working on Datavision and Veeva (preferred)
• A self-motivated, independent, and proactive personality
• Proper knowledge of GPP3 and other publication guidelines