Head Scientific Medical Services Hub
Galderma · Mumbai, India
Free account: apply link, HR contact and an AI-written cold email
Galderma · Mumbai, India
Free account: apply link, HR contact and an AI-written cold email
Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else. At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. Career Stream Tasks This role oversees the end-to-end preparation of: Peer-reviewed manuscripts, Congress abstracts, Scientific posters and oral-presentation materials, Consensus papers and expert recommendations Other scientific communication deliverables supporting Galderma’s Therapeutic Dermatology, Injectable Aesthetics and Dermatological Skin care Portfolio. The combines advanced medical-writing and publication-planning expertise with a strong understanding of medical design, data visualization, submission requirements, and publication governance. GPP 2022 applies to company-sponsored peer-reviewed and peer-oriented publications, including manuscripts, abstracts, posters, and meeting presentations. The position leads medical writers and medical-design professionals, supports their development, and strengthens the team’s capabilities, processes and Provide senior-level scientific and editorial direction throughout publication development, from concept and data interpretation through author review, submission, revision, and final publication. Applies 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. Monitor evolving requirements affecting biomedical publication, including artificial-intelligence policies. The January 2026 ICMJE recommendations state that AI technologies should not be listed as authors and that users should disclose the tool used and its purpose. Ensure publication objectives, scientific narratives, audiences, target journals, and congresses are clearly defined. Develop and maintain publication plans, timelines, priorities, resource forecasts, and delivery metrics. Anticipate publication risks, dependencies, and competing priorities, escalating issues and recommending practical solutions. Establish appropriate quality-control processes for scientific accuracy, data consistency, reference integrity, document versioning, design quality, and submission readiness. Ensure design choices strengthen scientific understanding without altering, overstating, or obscuring the underlying evidence. Confirm that final materials meet journal or congress specifications for dimensions, orientation, file format, resolution, font size, figure preparation, naming conventions, and upload requirements.
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