for a Medical Communications Writer The ideal candidate must have a strong background in medical and scientific writing, especially the medico-marketing/marketing communications. He/she must have a deep understanding of the pharmaceutical, life-sciences, medical devices and healthcare industry, and the ability to understand complex information and create a clear and an engaging content. As a Medical Communications Content Writer, he/she will play a critical role in our efforts to deliver high-quality communication materials that support our clients\' goals. Key Responsibilities: \xef\x82\xb7 Content Development: Ability to read and understand the project brief, guide the content writers and cross-functional teams on scope of work. Research, write, and edit a wide range of medical communication materials, including scientific manuscripts, medical marketing collateral, and educational content. Candidate must have a complete knowledge on the different types of marketing collaterals and best practices in creating such engaging content. He/she must be able to create content outline, storyline, and create/adapt the content to align the business/marketing objective, campaign plan and communication objectives. Review and proofread the content for quality & accuracy. Different types of collaterals he/she must be able to create include: o Print materials - Brochures, POS material, posters, newsletters, patient cards etc. o Digital materials - Emails, iDetails, E-learning modules, social media posts, slides, PPTs etc. o Audio-visual material - Educational videos, MoA Videos, 2d/3d animations etc. \xef\x82\xb7 Scientific Accuracy: Must have a deeper understanding of medical science (subject matter expert) and must ensure the accuracy, integrity, and scientific rigor of all content by staying upto-date with the latest developments in healthcare, pharmaceuticals, and relevant therapeutic areas. \xef\x82\xb7 Audience Adaptation: Write/adapt/customize the content to diverse target audiences, including healthcare professionals, patients, and regulatory authorities, while maintaining scientific integrity and regulatory compliance. \xef\x82\xb7 Collaboration: Collaborate with cross-functional teams, including medical experts, graphic designers, digital coding experts, project managers, clients & client servicing teams, to produce cohesive and effective communication materials. Liaise directly with clients and external stakeholders as required for the project. \xef\x82\xb7 Regulatory Compliance: Adhere to industry guidelines, regulatory requirements, and ethical standards to ensure all content meets the highest standards of quality and compliance. \xef\x82\xb7 People & Project Management: Manage multiple projects simultaneously, ensuring that they are completed on time and within scope. Work closely with peers & colleagues from content writing team; review the content created by fellow team members. \xef\x82\xb7 Feedback Integration: Incorporate feedback from clients and internal stakeholders to continually improve and refine content. \xef\x82\xb7 Content Approval Support: Must be aware of different types of submissions involved in content approval by clients/regulatory bodies/healthcare authorities preferably the US and UK. Knowledge on the submission process in other regions including EU, middle east & Asian markets is a plus. Hands of experience on Veeva Vault PromoMats is mandatory. Qualifications & requirements: \xef\x82\xb7 Masters degree in a relevant field (e.g., life sciences, pharmacy) is required. Advanced degrees (e.g, PhD) is a plus. \xef\x82\xb7 \xe2\x89\xa53 years of experience in medical communications (preferably medico-marketing/promotional content), medical writing, or a related field. \xef\x82\xb7 Strong understanding of the pharmaceutical and healthcare industry, including knowledge of clinical trials, drug development, regulatory processes, and marketing activities. \xef\x82\xb7 Exceptional writing and editing skills, with the ability to convey complex scientific concepts in a clear and engaging manner. Ability to edit the content for language, grammar, standard styles, referencing styles etc. \xef\x82\xb7 Proficiency with industry-specific software and tools (e.g., Microsoft Office, EndNote, and reference management software, Veeva Vault, Aprimo etc). \xef\x82\xb7 Strong attention to detail and ability to work independently or as part of a team. \xef\x82\xb7 Knowledge of industry guidelines, including ICH-GCP, PhRMA, and CONSORT, is a plus. \xef\x82\xb7 MUST be ready to work in different time zones as per the business need. Immediate need is to support the business in between 2:00 PM to 11:00 PM IST.Job Type: Full-timeSchedule:

• Day shift
• Rotational shift

Experience:

• total work: 3 years (Preferred)

Work Location: In person