113 Scientific Writing Jobs - Page 5

Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly. The purpose of the Scientific Communications Associate - Regulatory role is to work with cross-functional, multidisciplinary teams to lead the development of documents intended for regulatory audiences (including, but not limited to, clinical study reports, briefing documents, regulatory responses, Investigational New Drug Applications, and marketing authorization applications). Minimum Qualification Requirements: Bachelor s degree in a scientific, health, communications, technology health related field. Demonstrated experience in technical/ regulatory scientific writing. Strong communication and interpersonal skills. Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process)

Title: Senior Associate Scientific Writing Date: 12 Mar 2025 Location: Bangalore, KA, IN We are a technology led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers. We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast track careers while you work with a team that is fueled by purpose. The combination of these will lead to a truly differentiated experience for you. If this excites you, then apply below. Senior Associate Scientific Writing 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 etc 4. 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 planning 6. 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 referencing 8. 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 requirement Participate in client calls as per project requirements Compliance to quality, confidentiality and security Adhere and follow quality systems, processes and policies Comply to training and specifications Quality Management Process Compliance to quality, confidentiality and security: 1. Adhere and follow quality systems, processes and policies 2. Comply to training and specifications Team Management Assisting and mentoring colleagues on the scientific formats required to review the documents Provide 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 project Provide 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 material 6. 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 OPPORTUNITY

Conduct comprehensive literature reviews to gather relevant scientific data and insights. Perform systematic literature reviews to support evidence-based decision-making processes. Prepare and contribute to the creation of Global Value Dossiers (GVDs), AMCP dossiers, and other strategic research documents. Collaborate with cross-functional teams to understand research needs and deliver high-quality, timely reports. Maintain a keen understanding of the latest trends, methodologies, and regulations within the life sciences and healthcare sectors. Synthesize and summarize complex information in clear, concise formats for both internal and external stakeholders. Assist in the preparation of presentations and documents for regulatory and market access purposes. Support flexible working arrangements to maintain a healthy work-life balance while delivering exceptional research output.

Role & responsibilities 1).Scholarly manuscripts screening and assessment 2). Perform manuscript integrity checks as per guidelines 3). Provide editorial assistance 4). Respond to authors, reviewers, editors and manuscripts related queries. 5). Prepare accurate, regular progress reports to provide performance overview for key stakeholders as required 6).Peer review Management Preferred candidate profile 1).Excellent English language communication skills are a must. 2). Good working knowledge of Microsoft Office applications, especially Outlook and Excel is required 3). Prior work experience in the field of scholarly publishing is preferred 4). Prior experience of working with Science, Technology, Engineering, Math/Medicine (STEM)[SSH] journals or magazine publishers is ideal. 5). Prior knowledge of handling online manuscripts submission and peer review management systems is a big plus. 6). Prior experience in laboratory based or STEM & SSH related desk based research is advantageous 7). Research publications: proven track record with at least one scholarly article publication is desirable 8). Ability to deal with challenging problems and proactively identifying additional customer support opportunities 9). Ability to work both independently and collaboratively is essential 10). Ability to independently organize, execute, manage and track all assigned tasks Perks and benefits

Position Title: Scientific Writer Team: Regulatory Science Operations Job Type: Contract Job Location: Hyderabad (Hybrid) Job Description This is an exciting opportunity for a highly motivated individual to join Regulatory Science as a Scientific Writer and to be part of the Regulatory Sciences Operations team. The Scientific Writing Team drafts study reports and study summaries to support regulatory submissions for both biotech and crop protection products. This role will have a high emphasis on analytical chemistry. Scientific Writers collaborate closely with stakeholders and customers including Study Directors and Monitors, Subject Matter Experts, Quality Assurance, Statisticians, and Global Registration Teams. Job Summary Draft high-quality study reports and study summaries to support regulatory submissions for both biotech and crop protection products (this role work with analytical chemistry reports primarily). Strong scientific writing skills and a background in science (specifically analytical chemistry) is needed for drafting reports. Perform quality control reviews on draft reports and/or raw data. An understanding of Good Laboratory Practice (GLP) is required. Develop new report templates, optimize processes, and assess stakeholder feedback for continuous improvement. Coordinate peer reviews and Quality Assurance audits, collate comments, and facilitate finalization of reports and audit responses. Communicate effectively with key stakeholders and customers. Partnership with stakeholders and customers to understand regulatory reporting requirements is important for success. Job Qualification MSc (with knowledge in chemistry, biochemistry, or analytical chemistry); industry experience is preferred. Other degrees may be considered if proficiency in critical skills is demonstrated. The ideal candidate will have experience in analytical chemistry Highly proficient in English, both spoken and written. Excellent verbal communication skills, which includes the ability to work effectively in a team environment. Excellent written communication skills, which includes strong keyboard and data entry skills and strong knowledge of Microsoft Word, Excel, Outlook, and Adobe Acrobat. Excellent attention to detail and ability to work on several projects simultaneously, efficiently, and independently. Excellent interpersonal skills with the ability to interact with a diverse set of stakeholders. Ability to work a partially-modified schedule to ensure overlap with our US-based teams, facilitating real-time collaboration and communication during key business hours.

The Executive - PMT will play a critical role in product management and marketing within the nutraceutical or Ayurvedic industry. The role requires strong expertise in scientific research, formulation, regulatory compliance, business development, and training. Department: Product Management Team (PMT) Experience: Minimum 2+ years Industry: Nutraceutical / Ayurvedic Educational Qualification: Master's or Bachelor's in Nutrition, Food Science, Dietetics, or M.Pharm or BAMS Location: Sector 65, Noida Work Timings: 9:00 AM 5:30 PM (Alternate Saturdays off) Key Responsibilities: 1. Business Development Developing formulation propositions and spec sheets. Handling NPDI (New Product Development & Introduction) processes. Preparing product presentations, scientific research, comparison tables, and marketing data. Assisting the BD team with various queries related to formulations and regulatory aspects. 2. New Product Development (NPD) Conducting technical research and feasibility studies for new product development. Coordinating with R&D and other teams for data collection and correspondence. 3. Regulatory Compliance Reviewing artwork, validating scientific claims, and ensuring compliance with regulatory guidelines. 4. Training & Development Conducting monthly training sessions for the BD and regulatory teams. Preparing training materials including PPTs, quizzes, and other learning resources . 5. Event Management Planning and managing events, sponsorships, and exhibitions . Booking stalls, overseeing fabrication, and providing branding materials. Managing bills, payments, and vendor coordination. 6. Social Media & Marketing Collaterals Providing content for brochures, flyers, and leaflets . Proofreading and ensuring accuracy in marketing or promotional materials. 7. R&D Coordination Conducting feasibility checks and gathering product information. Collaborating with the R&D team for product development insights. 8. Business Development (Domestic & Exports) Attending client meetings and supporting the BD team with technical expertise. Assisting in market analysis, competitive research, and strategy development . Key Skills & Competencies: Strong knowledge of Nutraceuticals, Ayurveda, and Functional Foods . Expertise in scientific research, product development, and regulatory compliance . Ability to create engaging presentations and conduct training . Experience in event planning and marketing support . Excellent communication and cross-functional collaboration skills . Interested candidates can apply by sending their CV to hr3@zeon.co.in with the subject line Application for Executive - PMT.

Skill required: Marketing Operations - Content Creation Designation: Copywriting Senior Analyst Qualifications: Any Graduation Years of Experience: 5 to 8 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designThe role will include research, industry-related topics (combining online sources, interviews and studies), writing clear marketing copies to promote products/services, preparing well-structured drafts using CMS/tools, proofreading & editing content before publication, coordinating with marketing and design teams to illustrate articles, conducting simple keyword research, using SEO guidelines to increase web traffic and identifying customers needs and gaps in the content and updating on website. What are we looking for? Technical Writing Medical Review Medical Monitoring Creative Design Content Curation Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications Any Graduation

Greetings from You & I Consulting! You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. Hirings for MNC : - Great Opportunity in Giant MNC .Grab the Opportunity to grow and explore We are hiring for: Medical Writer CTC : upto 17 LPA Mode : Work From Office Location- Mumbai, Pune, Bengaluru Preferred experience for the role: • Overall ~5 years of authoring/editing experience in medical writing domain across different therapeutic areas in clinical documents including clinical study protocol, pediatric investigation plan, informed consent document, clinical study report, investigators brochure, clinical summary of pharmacology, clinical overview (efficacy and safety), briefing package/pre-meeting package preferred • Good knowledge of clinical research domain, ICH GCP principles, Common Technical Document (CTD) structure and regulatory requirements • Experience in preparation of clinical documents necessary for national and international regulatory submissions to the US, European and other regulatory agencies • Computer Literate: Knowledge of MS Word, PowerPoint, Adobe Acrobat, MS Excel, etc Responsibilities: • Setting, discussing and meeting expectations of the document during kick off and subsequent meetings Lead the authoring/editing of clinical documents, as mentioned above. Ensure adherence to established processes, timelines, regulatory guidelines and applicable standards, styles, guidelines Perform quality review of the clinical documents within established timelines with adherence to applicable guidelines, templates, and processes Ability to effectively and proactively communicate with internal and external stakeholders, including authors and key opinion leaders as appropriate (including problem-solving and resolution of issues) • As required, take on functional role and responsibilities of the role of Documentation Lead o Lead PDRD deliverables for project and act as first point of contact for any information that is required for content/document preparation Ensure alignment and content re-use across documents for a product Onboard lead document writers on document content alignment and timelines. Provide required source documents incl. information pertaining to study documentation, relevant project contacts (authors, reviewers), developmental strategy Actively participate in Regulatory Affairs Functional or other cross functional team meetings Review content of document prior to finalization to ensure high quality prior to initiation of author review or Expert Team Review Perks and benefits: ONLY 5 Days Work CAB Fecility Medical Benefits To Apply Call on 8250242229 (Puja) / Whats app on the same Number ***Though We Try and Answer The Calls Immediately, but Due to Heavy Call Flow The Below Numbers Might Be Busy At Times. In case you find the number busy, please WhatsApp your details to us in the below format: - 8250242229 (Puja) Name- Mobile number - Mail - Highest Qualification Highest qualification University Name Total work experience - Date of birth- Current Organization- Preferred Location Last CTC- Expected CTC: *Interested candidates can even refer their friends or relatives provided the criteria *FOR interview Call Now our HR Specialist: -----@ ** 8250242229 (Puja) (call or WhatsApp)

Position Title: Scientific Writer Team: Regulatory Science Operations Job Type: Contract Job Location: Hyderabad (Hybrid) Job Description This is an exciting opportunity for a highly motivated individual to join Regulatory Science as a Scientific Writer and to be part of the Regulatory Sciences Operations team. The Scientific Writing Team drafts study reports and study summaries to support regulatory submissions for both biotech and crop protection products. This role will have a high emphasis on analytical chemistry. Scientific Writers collaborate closely with stakeholders and customers including Study Directors and Monitors, Subject Matter Experts, Quality Assurance, Statisticians, and Global Registration Teams. Job Summary Draft high-quality study reports and study summaries to support regulatory submissions for both biotech and crop protection products (this role work with analytical chemistry reports primarily). Strong scientific writing skills and a background in science (specifically analytical chemistry) is needed for drafting reports. Perform quality control reviews on draft reports and/or raw data. An understanding of Good Laboratory Practice (GLP) is required. Develop new report templates, optimize processes, and assess stakeholder feedback for continuous improvement. Coordinate peer reviews and Quality Assurance audits, collate comments, and facilitate finalization of reports and audit responses. Communicate effectively with key stakeholders and customers. Partnership with stakeholders and customers to understand regulatory reporting requirements is important for success. Job Qualification MSc (with knowledge in chemistry, biochemistry, or analytical chemistry); industry experience is preferred. Other degrees may be considered if proficiency in critical skills is demonstrated. Hands-on experience in different HPLC (or analytical) techniques, Interpret the test results with high accuracy from the raw data. Knowledge on writing protocols/ reports based on study (HPLC or other analytical test) findings. 2 to 7 years of relevant experience The ideal candidate will have experience in analytical chemistry Highly proficient in English, both spoken and written. Excellent verbal communication skills, which includes the ability to work effectively in a team environment. Excellent written communication skills, which includes strong keyboard and data entry skills and strong knowledge of Microsoft Word, Excel, Outlook, and Adobe Acrobat. Excellent attention to detail and ability to work on several projects simultaneously, efficiently, and independently. Excellent interpersonal skills with the ability to interact with a diverse set of stakeholders. Ability to work a partially-modified schedule to ensure overlap with our US-based teams, facilitating real-time collaboration and communication during key business hours.

Hi, We are hiring for Leading ITES Company for Medical Writer Profile. Role & Responsibilities: Prepare and review clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, and Post Approval Documents across the Therapeutic Areas. Quality check of the clinical documents that are part of regulatory submission including but not limited to Protocol, Clinical Study Pharmacology Report, Clinical Study Report, Narratives, Clinical Summary of Safety, Clinical Summary of Efficacy and Common Technical Document Modules. Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission, if required. To work in coordination with all the members in the study team- internal and external for the development of clinical documents. Share project timelines amongst the study team for the development of document. Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and Guidance document. Review statistical analysis plans and table/figure/listing, when required. Ensure uniformity and consistency in the scientific content of the regulatory documents Preparation of documents in the scope and other Medical Writing documents that may be required for domestic and international regulatory submissions to the US, European, and other regulatory agencies. Prepare Medical Writing documents within established timelines that are of high quality for scientific content, organization, clarity, accuracy, format, and consistency, with adherence to regulatory guidelines and applicable standards, styles, guidelines, and processes. Perform peer review and quality control review of the documents within established timelines with adherence to applicable guidelines, and processes, using appropriate checklists. Take an active role on assigned projects with respect to planning of content, format, and timing of documents, report scheduling/tracking, etc. Provide support to the assigned clinical development or project team to ensure that project needs, and department standards are met, while completing reports within established schedules/timelines. Plan and organize project and non-project meetings, as and when required To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Medical Writing Mumbai (Job Code # 56) b) For Position in Pune Search : Medical Writing Pune (Job Code # 57)

About Strand Life Sciences: Strand is a 24-year-old spin-off from the Indian Institute of Science. We are a cutting-edge Genomics company with a global customer base. We build applications that use DNA sequencing to improve human health. In the process, we build algorithms, data pipelines, and visualizations to handle large amounts of sequence data. We are committed to transforming complex data into actionable insights, contributing to groundbreaking research and innovative solutions in the field of genomics. We anticipate that in the next few years, hundreds of millions of individuals will have their DNA sequenced, and invite you to join us in this transformative journey. About the Position We are looking for a talented and creative Content Creator/Writer to develop compelling, engaging, and high-quality content across various digital platforms. The ideal candidate should have a strong command of language, a knack for storytelling, and the ability to create content that resonates with the target audience. Key Responsibilities: Research and develop long-form and short-form digital content such as case studies, white papers, brochures, blogs, LinkedIn posts, etc Perform literature reviews on various bioinformatics and genomics technologies and develop informative blogs/social media posts. Regularly interact with internal project teams to stay up to date on products and services Proven ability to translate complex scientific concepts into engaging content for different audiences Resourceful, organized, and motivated to enhance sales opportunities, and look for new and creative ways to expand our client portfolio. Collaborate with technical, design, and sales teams to align content with brand guidelines and strategy. Repurpose long-form content into bite-sized posts, infographics, and videos for multiple channels. Conduct interviews, write case studies, and develop thought leadership articles. Conduct research on industry trends and competitor analysis to inform and optimize content development efforts. Stay updated with the latest content marketing trends and digital storytelling techniques. Requirements: Masters (2-3 Years Exp.) or PhD (0-2 Years Exp.) in Life Sciences, Biotechnology, or a related field from a reputed institute Proven experience in content writing, copywriting, or content marketing in genetics. Excellent writing, editing, and proofreading skills with a strong attention to detail. Ability to write for different audiences and adapt tone and style accordingly. Familiarity with content management systems (CMS) such as WordPress. Basic knowledge of design tools like Canva or Adobe Suite is a plus. Strong time management skills with the ability to meet deadlines. Preferred Skills: Experience in writing for specific industries (e.g., biotech, pharma, diagnostics). Knowledge of social media marketing and content distribution strategies. Ability to create video scripts and multimedia content. Understanding of SEO best practices and content optimization techniques. We offer An innovative and open culture in a truly multicultural environment An opportunity to make a fundamental impact on human health Vibrant multidisciplinary scientific interaction and learning opportunity A collaborative and solution-oriented environment where you can make a difference A competitive salary and generous benefits

Responsibilities Are you interested in working in one of the most impactful areas of technology in the world today? Do you want to build generative AI skills while working on a project to transform the most mission-critical IT workloads for organizations that power the global economy? Come join the team that is at the intersection of cutting-edge gen AI and mainframe software development, a key strategic pillar for IBM. This role is tailor-made for mainframe professionals eager to embrace the future, and you'll work at the crossroads of trusted mainframe technology and the transformative potential of AI, building solutions that power enterprise modernization. As a Gen AI Model trainer you will create training material which will be used to train an LLM on how to explain or transform code. This training material will be used to aid conversion from source language to English or other industry standard language. Futhermore, you will involve in Model ranking and advice on Model improvements and prompting. Required education Bachelor's Degree Preferred education Master's Degree Required technical and professional expertise 5+ years of Industry experience Minimum of 5 years of recent industry experience programming in PL/I Outstanding communication and collaboration skills Demonstrated ability to work with remote teams Preferred technical and professional experience Any prior COBOL/Java/HLASM programming experience Exposure to Agile methodology Experience with program analysis. This would involve working with static analysis information, abstract syntax trees, control flow graphs, and variable dependency analysis. Exposure to LLMs and prompt engineering

Responsibilities Are you interested in working in one of the most impactful areas of technology in the world today? Do you want to build generative AI skills while working on a project to transform the most mission-critical IT workloads for organizations that power the global economy? Come join the team that is at the intersection of cutting-edge gen AI and mainframe software development, a key strategic pillar for IBM. This role is tailor-made for mainframe professionals eager to embrace the future, and you'll work at the crossroads of trusted mainframe technology and the transformative potential of AI, building solutions that power enterprise modernization. As a Gen AI Model trainer you will create training material which will be used to train an LLM on how to explain or transform code. This training material will be used to aid conversion from source language to English or other industry standard language. Futhermore, you will involve in Model ranking and advice on Model improvements and prompting. Required education Bachelor's Degree Preferred education Bachelor's Degree Required technical and professional expertise 3+ years of experience of Industry experience. Minimum of 3 years of recent industry experience programming in PL/I Outstanding communication and collaboration skills Demonstrated ability to work with remote teams Preferred technical and professional experience Any prior Java/COBOL/HLASM programming experience Exposure to Agile methodology Experience with program analysis. This would involve working with static analysis information, abstract syntax trees, control flow graphs, and variable dependency analysis. Exposure to LLMs and prompt engineering