Scientific Writer
3 weeks ago
Senior Associate Scientific Writing
Job Description:
1. Working with clients & PM team to understand the project requirements, create content plan for the deliverable as per the target audience & objective, provide solution for queries and work with internal cross-functional teams and providing directions to graphic designing team in developing the creative elements such as images/visuals/interactivities/animations.2. Understand the structure and flow of content to re-organize the same for further use, as required.3. Developing & reviewing the scientific content for promotional literature and medico-marketing solutions such as promotional emails, patient/physician brochures, newsletters, product/drug monographs, digital & print channels, visual aids, websites, social medial channels etc4. Developing innovative scientific content for physicians, pharmacists and patients on medicinal products, diagnostic devices, disease management guidelines, by leveraging their in-depth understanding of medical/scientific content.5. Project planning6. Ensure that medical content delivered is rated high on depth, comprehensiveness, quality and timelines interfacing with clients on a regular basis.7. Working knowledge on digital campaigns, creating content strategy & defining multi-channel tactics for these campaigns is a plus.Responsible to follow the best practices in the department regarding - processes, communication (internal & external), project management, documentation and technical requirements like - language, grammar, stylization, content search, summarizing, data conflicts and referencing8. Attention to detail in reviewing the scientific manuscripts in terms of scientific accuracy, referencing, language, communication tone as per target audience and the delivery channel.9. Participate in assigned training programs and work on assignments as per requirementParticipate in client calls as per project requirementsCompliance to quality, confidentiality and securityAdhere and follow quality systems, processes and policiesComply to training and specifications
Quality Management & Process Compliance to quality, confidentiality and security:1. Adhere and follow quality systems, processes and policies2. Comply to training and specificationsTeam Management - Assisting and mentoring colleagues on the scientific formats required to review the documentsProvide guidance and support to all team members on a project with regard to format, style, content, and compliance.Guide and mentor team members to ensure consistency and completeness of the projectProvide peer review for colleagues in support of all documents
Must Have:
1. Minimum 3 to 4 years of experience in pharmaceutical companies in pharma marketing.2. Prior experience of minimum 3 years in content development & reviewing for scientific accuracy, legal compliance for marketing collaterals/promotional writing, probably those with experience in writing the content for blogs, websites, advertisement industry. Experience in developing and reviewing promotional content is MANDATORY. 3. Understanding on medico-legal-regulatory review processes, Veeva Vault/ZINC systems is preferred.4. Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field.5. Quick analysis of the content structure/flow of any medical training/ marketing material6. Strong flair and passion for writing.7. Strong written and verbal communication/presentation skills. Perfect organization skills.8. Passion for networking.9. Being up-to-date with the latest technical/scientific developments and relating them to various projects.
Good to have:Collaborate with clients and PM team to understand project requirements and create content plans. Guide graphic design for creative elements. Create, review, reorganize content as needed. Develop and review scientific content for promotional materials, ensuring accuracy and quality. Ideate and develop content for medical products and disease management. Plan projects and ensure timely delivery. Understand digital campaigns and create content strategies. Follow best practices, maintain high standards, and mentor team members. Participate in training and adhere to quality and compliance guidelines.
Develop and review scientific content for marketing and promotional materials, ensuring accuracy and legal compliance. Mandatory experience in promotional content development. Preferred knowledge of medico-legal-regulatory review processes and systems like Veeva Vault/ZINC. Understanding of a medical specialty or general medical field. Ability to quickly analyze content structure. Strong writing, communication, and organizational skills. Passion for writing, networking, and staying updated with scientific developments.
EQUAL OPPORTUNITYIndegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
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