Content Writer

• To perform quality control activities, ensuring the accuracy of all information, data, and references for the documents/tables/figures/listings produced, also reviewing spelling, grammar, appropriateness of language, correct mention of links to other parts of the document or other documents, and compliance with industry guidelines.
• To check information in the document against the data source (internal consistency within a document and across documents).
• To deliver documented quality review comments or checklists to the document’s author through resolution, while interacting with the Medical Writers and other team members to resolve QC findings.
• To liaise with internal groups such as Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, Clinical, and Quality Assurance to gather necessary information.
• To ensure timely completion of quality control activities and keep the Medical Writer (MW) informed of document status in relation to quality and timelines.
• To maintain familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing and quality control.

Quality Control Specialist – Medical Writing

• Write well-researched blogs, website/landing page content, and press articles.
• Research and place primary, secondary, and LSI keywords strategically.
• Make content interesting while naturally including relevant keywords.
• Optimize content for search engines using on-page SEO techniques.
• Write compelling meta titles and descriptions.
• Optimize headers (H1, H2, H3), image alt text, and URLs.
• Proofread and edit content for grammar and clarity.
• Create social media posts, official emails, and any other content required by the team.

Content Writer Intern

• Write and edit high-quality long-form and short-form content across multiple formats.
• Develop thought leadership articles, bylined pieces, whitepapers, reports, blogs, case studies, website copy, and executive opinion pieces.
• Create concise content including press releases, media pitches, social media copy, newsletters, emailers, and messaging documents.
• Research industry trends, technology innovations, and corporate developments to create relevant and engaging content.
• Collaborate with account teams to understand client objectives and translate them into impactful content.
• Adapt tone, style, and messaging for different industries, audiences, and communication channels.
• Ensure all content is accurate, well-structured, grammatically sound, and aligned with brand guidelines.
• Manage multiple projects simultaneously while meeting tight deadlines.

• Create compelling short-form scripts (under 60 seconds) with strong storytelling flow.
• Translate content from Regional Language to English and English to Regional Language.
• Write sharp, attention-grabbing hooks to maximize engagement and retention.
• Craft platform-specific content for Instagram, YouTube, Facebook, and other channels.
• Analyze ad metrics (CTR, watch time, drop-off rates) to refine creative strategy.
• Collaborate closely with video editors, designers, and creative strategists to bring ideas to life.
• Translate copy ideas into strong visual narratives and impactful storytelling sequences.
• Identify and adapt to emerging content and creative trends.
• Simplify complex ideas into relatable and emotionally resonant content.
• Constantly read and watch diverse content (books, short films, ads) to expand creative vocabulary and visual literacy.
• Provide creative inputs during production to ensure content quality and tone consistency.

Script Writer – Kannada

Script Writer – Telugu

• Supervises Medical Writers. Provide short-term and long-term resource planning in order to assign projects to appropriate and available staff. Holds regularly scheduled meetings with staff and provide updates to senior management. Review and approve semimonthly time sheets. Assist staff to forecast project-related costs and timelines for completion. Hires and evaluates employees. Recommends salary levels and promotions
• Supervises the preparation of Medical Writing deliverables. Organizes processes for completion of projects within established timelines. Evaluate timeliness and quality of deliverables and provides updates to senior management. Acts as a resource for questions relating to study design, adverse event reporting, and statistical analyses. Assists writers in presentation and interpretation of data. Performs senior review to ensure overall adherence to departmental standards. Write and review group SOP and WPD. Evaluates compliance with SOP/WPD on an ongoing basis. Stays updated on the guidelines and requirements of the ICH, FDA and other relevant agencies.
• Gives marketing presentations to potential clients on the capabilities of the Medical Writing department. Interacts with Bids and Contracts and Business Development to prepare proposals for Medical Writing projects.
• Develops and maintains training programs for Medical Writing. Ensures that all writers are adequately trained.
• Uses clinical knowledge to assist in the written interpretation of clinical data and to guide others in their presentation of clinical data.
• Writes and coordinates other documents for submission to regulatory agencies, including IND, NDA, and CTD items.

Manager, Medical Writing

• Responsible for the preparation and review of aggregate safety, risk management, and signal detection documents.
• Perform report management activities and lead client communication for the assigned reports.
• Assist other medical writers in their safety deliverables, act as a co-author for complex or large reports.
• Provide oversight and quality review of reports prepared by peers or junior associates.
• Conduct scientific literature searches and review for safety reports or routine surveillance activities.
• Ensure timely delivery of high-quality documents to internal customers and sponsors/clients.
• Foster excellent working relationships with all clients, both internal and external, with the highest quality of service in a cost-effective manner on time, every time.
• Write various safety reports (or part of such reports) for global regulatory submissions, including but not limited to Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Development Safety Update Report, Risk Management Plans, and other documents.
• Take ownership of the assigned deliverables and collaborate with internal/client stakeholders and the client to get the required inputs.
• Perform quality review of the safety reports prepared by junior or associate medical writers.
• Author or contribute to ad hoc reports, benefit-risk evaluation reports, justification/supporting documents for label updates.
• Write Common Technical Document Summaries including Non-Clinical and Clinical Overviews, Clinical Summaries and other regulatory documents as assigned.
• Prepare medical information responses for HCPs.
• Author/contribute to signal reports (ad hoc and periodic) and safety issue analysis reports.
• Write subject narratives for adverse drug reactions and serious adverse events.
• Internal and external (client) communication and co-ordination to get the required inputs.
• Participate in creating and updating labels, e.g., Core Data Sheets, USPI, centralized SPCs, Med Guides.
• Conduct literature searches for authoring several types of reports or routine surveillance activities.
• Review and propose updates needed if any to the search strategies.
• Review the articles selected by other medical writers/junior writers.
• Author literature abstracts/summaries and propose Company comments.
• Implement and promote use of consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard operating procedures and assume accountability for the deliverables.
• Ensure compliance of operations with governing regulatory requirements.

Safety Writer

• Develop, curate, and maintain high-quality proposal content and supporting materials for Oracle Cloud solutions, ensuring accuracy, consistency, and compliance with client requirements.
• Work closely with our capture management team to develop, refine, and deliver the most current and relevant proposal/orals content—including content and diagrams related to Oracle Cloud services—tailored to specific opportunities.
• Partner with delivery teams to define and draft content for new Oracle Cloud services and unique solutions for inclusion in upcoming proposals.
• Ensure all proposal content and graphics, particularly those relating to Oracle Cloud, follow established review processes and internal toll gates, maintaining a high standard of proposal content quality and organization.
• Maintain all proposal content in an organized, easily accessible manner within Microsoft Teams.

Proposal Writer

• Lead end-to-end signal management activities
• Perform and oversee qualitative and quantitative signal analysis
• Ensure compliance with global pharmacovigilance regulations
• Provide oversight and author aggregate safety reports
• Manage timelines, resources, budgets, and risks
• Supervise and mentor line reports

Senior Manager, Medical Writing Services

• We're looking for a Content Marketing Intern to help manage our publishing workflow.
• This is a foundational role within the Content & Marketing team, where you'll work closely with writers, SEO specialists, and team leads to ensure content goes live accurately, consistently, and at the quality bar we expect.
• Your main responsibility will be uploading and formatting content on our CMS while ensuring every page meets our quality standards. This includes checking SEO fundamentals, spotting editorial issues, and flagging gaps before content goes live.
• You'll do some light editing and refinement where needed, but your focus is being a quality gate: catching what's broken, what's missing, or what doesn't align with our template and brand voice.
• You'll also support the wider content team with operational tasks such as auditing pages, maintaining documents, and running process-driven work that keeps things moving.
• This isn't just about publishing pages. You'll learn how content operations, SEO, and publishing workflows work together at scale, and how strong systems keep a global content engine running smoothly. You'll contribute real work from week one and build hands-on exposure to how high-quality content gets shipped across a fast-moving marketplace.

Intern, Content Writer

• Collaborate with Sales partners to produce complex, high quality proposals
• Manage overall project requirements and milestones
• Communicate proactively and coordinate internal strategy meetings
• Outsource questions, format documents, create compliance-approved custom content, and provide document quality review
• Oversee project milestones and ensure output is consistent with all required proposal standards and business objectives
• Coordinate final document distribution and ensure external deliverables are met
• Train and mentor team members, and serve as a resource for market-specific support
• Clearly articulate challenges through verbal and written communication
• Collaborate with business partners to deliver consistent messaging in the marketplace
• Assist with internal content library maintenance
• Update internal tracking systems for real time reporting purposes
• Lead and serve as a key contributor on cross-functional projects and process enhancements

Senior Writer, Marketing RFP

• Collaborate with Sales partners to produce comprehensive, high quality proposals
• Manage overall project requirements and communicate proactively
• Coordinate internal strategy meetings and outsource questions
• Format documents and oversee project milestones
• Ensure output is consistent with required proposal standards and business objectives
• Support a range of project complexities
• Perform review of proposals to ensure accuracy of data

Writer, Marketing RFP

• Produce 10+ B2B news articles daily by researching targeted industries and companies using assigned sources and databases.
• Monitor industry news, analyze financial/advertising data, and compile trend reports for content production and actionable sales leads.
• Execute basic database entry to log, organize, and maintain research data.
• Edit your own work and review others' output for clarity, data accuracy, and seamless workflow efficiency.
• Strictly follow AP Style and in-house editorial guidelines for all written content across both US and UK English audiences.
• Coordinate closely with Researchers, Marketing, and Product teams to ensure all content accurately meets customer needs.
• Use project management and data tools (Airtable, Google Workspace, internal databases) to streamline research and log data.
• Assist with product development initiatives related to AI/LLM tools, content automation, and workflow improvements.
• Continually refine your research techniques to enhance overall content and data quality.

Newswriter I

• Providing key contributions to clinical document strategy for one or more assets throughout the life cycle of drug development
• Documents in scope include, but are not limited to, clinical study protocols, clinical sections of the IMPD/IND, Investigator’s Brochures, clinical study reports, briefing documents for regulatory authorities, Common Technical Document Summaries and Clinical Overviews, and responses to regulatory authority questions
• Leading matrix teams in planning and production of multiple clinical documents, working with CROs and/or independent contractors as needed
• Planning and successfully delivering large submissions independently, effectively recommending innovative methods and solutions for achieving accelerated timelines
• Assessing and adapting to interdependences of various contributing functions and managing problems affecting timelines as necessary
• Ensuring a global approach for submissions as appropriate, collaborating with Global Regulatory Affairs to ensure business needs and regulatory requirements are met
• Providing guidance and facilitation to submission teams in development of detailed submission plans
• Acting as lead author on submissions
• Effectively organizing content and arguments in complex clinical submission documents, including briefing documents and responses to regulatory questions
• Proposing resourcing solutions for major projects including the number of FTEs required and best use of internal and external resources
• Actively contributing to development of training materials for therapeutic area and providing mentoring and/or training on regulatory requirements, medical writing processes, and submission planning to individuals or teams
• Driving, promoting and implementing key organizational process improvement initiatives
• Proactively generating ideas for simplification and improvement taking advantage of opportunities that arise and challenging the status quo
• Prioritizing and meeting multiple deadlines successfully with attention to detail, demonstrating high performance standards for own work and encouraging similar standards across the matrix
• Promoting leadership behaviors that support GSK values.

Director, Medical Writing Asset Lead

• Write clear, attractive copy, adapted to specific target audiences - i.e., matter-of-fact writing, not marketing fluff.
• Interpret marketing briefs to understand project requirements.
• Collaborate with marketing team members (graphic designers, content marketing manager, social media manager, email marketer, webmaster, etc.) on large- and small-scale marketing projects (e.g., email campaigns, landing pages, case studies, brochures, sales presentations, video scripts, etc.)
• Edit and proofread copy to ensure high quality standards are met.
• Conduct high-quality research and interviews.
• Use SEO principles to maximize content’s performance on search engines.
• Drive brand consistency across company communications.
• Apply brand guidelines/voice.

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