518 Scientific Writing Jobs - Page 5

Responsibilities Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client and audience needs with excellent attention to detail. Actively involved in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervisi...

Summary Creation of high-quality highly-complex scientific content, such as publications and foundational core content elements, in line with priorities and scientific narrative defined in SCP. Ownership of content from brief to publication or presentation, for first-time right delivery About The Role Principal Scientific Writer Location Hyderabad Hybrid About The Role: Working in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand, this role will be responsible for delivering and supporting scientific excellence of Medical Communications services across their accounts Key Responsibilitie...

As a Medical Writer, you will be responsible for preparing, reviewing, and editing reports, manuscripts, drug monographs, medico-marketing material, systematic reviews, and meta-analysis on varied disease domains. Additionally, you will handle projects in regulatory writing, including protocols, clinical study reports, patient consent forms, case report forms, and other related activities. Key Responsibilities: - Prepare and review reports on disease background, epidemiology, outcomes, and disease burden in oncology and non-oncology domains - Conduct literature survey/searches for HEOR/RWE studies and other published literature from electronic databases - Prepare documents for value communic...

As an Associate Manager at our company, you will be responsible for developing various types of medical affairs content under the supervision and support of your manager. Your key responsibilities will include: - Developing relevant medical affairs content such as abstracts, manuscripts, congress posters/presentations, graphical abstracts, systematic literature reviews, plain language summaries, slide decks, medical education resources, social media, infographics, video, and multi-media. - Researching, organizing, compiling, interpreting, and quality checking various types of technical and/or medical content. - Providing solutions to stakeholders in alignment with your manager for all projec...

Key Responsibilities: ? Content Research & Curation: Identify, verify, and prepare relevant biotech/life science opportunities, updates, and resources for our audience. ? Article Writing: Create engaging career guidance articles tailored to students and professionals. ? News & Research Summaries: Curate and simplify the latest developments in biotechnology, life sciences, and allied fields. ? Creative & Media Support: Assist in designing presentations, brochures, posters, infographics, and social media creatives. ? Engagement & Outreach: Ensure all content is clear, accurate, and engaging to connect effectively with readers. Digital Skills and Tools Utilization: ? Social Media Engagement: Ut...

Main responsibilities: The overall purpose and main responsibilities are listed below: To create/review complex and specialized content (branded/unbranded) without supervision; manage end-to-end Omnichannel content creation/repurposing/localization process including supporting designing & enhancement, validation, tagging & upload, deployment, publishing, and dissemination via relevant tools & platforms. Develop and maintain therapeutic area(s), process(es), and compliance expertise for Omnichannel pillar/GTMC. Support background research/literature analysis/due diligence and application of available content insights generated via AI-enabled digital platforms, Search Engine Optimization (SEO)...

We are looking for a highly motivated and detail-oriented individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records, including diagnoses, treatments, and test results. Analyze medical data to identify trends, patterns, and areas for improvement. Collaborate with healthcare professionals to develop and implement effective treatment plans. Maintain accurate and up-to-date records of patient information and review findings. Participate in quality improvement initiatives to enhance patient care and outcomes. Develop and maintain knowledge of medical ...

Looking for a motivated individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records and reports. Analyze data to identify trends and patterns, providing insights for informed decision-making. Collaborate with healthcare professionals to develop effective treatment plans. Stay updated on the latest medical research and developments. Maintain accurate and detailed records of review findings and recommendations. Participate in quality improvement initiatives to enhance processes and outcomes. Job Requirements Strong understanding of medical terminolog...

You will play a crucial role in the Advanced Data Science team within the Data Sciences organization, focusing on fostering scientific excellence in digital biomarkers and endpoints. Your main responsibilities will include: - Leading the identification, development, and implementation of innovative digital endpoints and outcome measures - Collaborating with the Global Digital Health organization to design and validate algorithms for extracting clinically relevant insights - Incorporating digital health technologies into evidence generation strategies to promote their adoption in clinical trials and medical practice - Contributing to key regulatory filings and publications advocating for the ...

As a member of the global Data Sciences organization, you will play a crucial role in establishing scientific excellence by developing digital biomarkers and endpoints. Your primary responsibility will be to lead the identification, development, and deployment of innovative digital endpoints and outcome measures for use in clinical trials and life cycle management programs. Collaborating closely with the Global Digital Health organization, you will be involved in designing and validating algorithms to extract clinically relevant insights from various digital health data sources, ensuring scientific rigor, clinical validity, and regulatory readiness. Key Responsibilities: - Lead the identific...

Role & responsibilities Medical Report writing for Medical Providers and Law Firms in USA. Drafting Rebuttals, Review report Drafting. Preferred candidate profile Science Graduates, Doctors and Pharmacists Perks and benefits

About The Role Skill required: Marketing Operations - Medical Affairs 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/designDesign, develop and deliver business solutions related to the medical affairs gr...

We are looking to add an experienced Clinical Writer to our team. The person in this position must be able to independently contribute to the development of initial and update(s) of CERs that support the applicable regulatory submission requirements for the medical device products. An experienced Clinical Analyst professional has relevant medical/life-science qualification and knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 7 - 8 years with a minimum of 4-5 years of CER writing experience is essential. A minimum of 4-5 years of medical writing/reviewing experience is needed. The experience is expected to be curren...

Job Requirements We are looking for an experienced Medical Content Writer to join our team at Torrent Diagnostics. In this role, you will be responsible for creating and editing content for our website, blog, and other digital platforms. You will be expected to research and write content that is accurate, engaging, and SEO-friendly. You should have a good understanding of scientific concepts and be able to explain them in a simple and concise manner. Additionally, you should be able to work independently and be able to meet tight deadlines. Responsibilities: Research and write content for our website, blog, and other digital platforms. Ensure accuracy and consistency of content. Ensure conte...

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile and Allergy Therapy Products, and Generics and APIs, comprising Solid Dosage Formulations and Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research and Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another a...

To manage and complete assigned Medical Communications deliverables at high quality standards and in accordance with agreed timelines Projects include manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning and medical education materials for internal medical and/or clinical teams About The Role Major Activities Demonstrate a command of assigned therapeutic areas and expertise with assigned products Research and write original content for publications activities (primary and review manuscripts, abstracts, posters), slide presentations and other materials based on direction and materials supplied by customers Prepare me...

You are being offered a dual role at Imagica Health as a Medical Writer cum Project Manager. In this position, you will be responsible for a variety of tasks in scientific writing and project management in pharma software. As a Medical Writer cum Project Manager at Imagica Health, you will spend 25% of your time on scientific writing tasks. This includes conducting scientific reference searches, selecting and evaluating relevant articles, assisting in brand strategy development, contributing innovative ideas, and creating engaging content for patient education materials. The remaining 75% of your role will be focused on project management in pharma software. You will be responsible for effec...

Education: Ph.D./M.Pharm/Pharm D or Any other Medical Degree Experience: 3+ years Position Requirements: Experience with pharmaceutical/medical writing experience, or an equivalent combination of related education and experience. Experience writing for the digital environment is preferred. Ability to analyse complex data and interpret it for mobile/web application while maintaining a clinical tone Ability to quickly distill complex information into essential elements relevant to clinicians at the point of care Excellent medical literature retrieval and evaluation skills Independent and innovative self-starter Should be familiar with use of databases like Pubmed, Ovid, Medical conference site...

Job Summary: We are seeking a highly skilled and motivated Scientific Content Writer to join our team. The ideal candidate will have a strong scientific background and a passion for communicating complex scientific concepts in a clear, concise, and engaging manner. This role involves creating high-quality content for various platforms, including research articles, white papers, blog posts, product descriptions. Key Deliverables: Content Creation: Write, edit, and proofread scientific content for various mediums such as websites, blogs, white papers, research articles, and marketing materials. Translate complex scientific data and research findings into accessible, reader-friendly content. Cr...

Key Responsibilities: Ideate and Execute campaigns for Digital Engagement to achieve the target numbers Keep up to date with the latest advances and news in the healthcare industry Campaign level reporting Making graphics for WhatsApp, SMS and Emails using various Software. Maintaining and updating the monthly Campaign Calendar/Planner. A/B testing of campaigns before shooting the main campaign Meeting Target set by the organization

Mahatma Gandhi Mission Hospital is looking for Clinical Coordinator to join our dynamic team and embark on a rewarding career journey Oversee clinical operations and ensure compliance with regulations. Coordinate patient care and clinical activities. Manage clinical staff schedules and assignments. Monitor and evaluate clinical performance. Develop and implement clinical policies and procedures. Collaborate with healthcare providers and administrators. Ensure high-quality patient care and satisfaction. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details...

Role & responsibilities Provide comprehensive medical and scientific expertise and oversight for clinical trials, ensuring study integrity and participant safety. Review and contribute medical input to study protocols, ensuring clinical feasibility, scientific rigor, and compliance with regulatory requirements and guidelines. Ensure strict adherence to clinical trial protocols through continuous monitoring and proactive management of ongoing studies. Prepare, critically review, and approve essential clinical trial documents across all phases, including Informed Consent Forms (ICF), Statistical Analysis Plans (SAP), Clinical Study Reports (CSR), Safety Management Plans, Medical Management Pla...

Role Overview: As a Medical Affairs Executive, your primary responsibility is to understand current practices, medicines, and trends in the respective therapeutic area by engaging in doctor visits, attending scientific symposia, and reviewing key therapeutic journals. This knowledge will enable you to provide valuable information to both internal and external customers. Key Responsibilities: - Publish scientific articles related to company products. - Create presentations for doctors for Continuing Medical Education (CME) sessions and product launches. - Participate in implementing the medico-marketing strategy. - Conduct regular field visits to doctors for product management and Key Opinion...

Job Description: As a Medical-Regulatory Writer Assistant Manager, your main responsibility will be to plan and manage Medico-Regulatory Writing in accordance with relevant Regulatory Guidelines. You will be expected to deliver high-quality medical and scientific writing, provide technical consultation and advice on strategy and regulations, demonstrate subject matter expertise, effectively manage writing projects to meet deadlines, collaborate with internal and external clients, and produce various types of reports including CTD Modules, Safety Reports, and Aggregate Reports. Key Responsibilities: - Conduct science reviews of aggregate reports - Ensure document compliance with client specif...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The Clinical Evaluation Medical Writer on our Endoscopy team plays a key role in developing and updating clinical evaluation documents (e.g., CEP, CER, PMCFP, PMCFR, SSCP) to support CE Mark submissions and maintain compliance throughout the product lifecycle. This work follows MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745 and involves close collaboration with cross-functional teams to gather and interpret data on device safety, perfo...