Senior Medical Writer

1 week ago

Bengaluru, Karnataka, India Lilly Full time

We're looking for people who are determined to make life better for people around the world.

Position Description:

The Senior Medical Writer Commercial Learning Services (CLS) is responsible for the development of medical content including but not limited to creating/updating wireframes, building reference packages, creating/updating learning content for product trainings for assigned areas at both Global and affiliate level. The Medical Writer will anticipate and adjust for problems and roadblocks, interface with Lilly partners at Indianapolis and LCCI and integrate new business processes where necessary. Using strong adult learning principles, Medical Writer ensures quality design, development, and delivery of training development projects. This role will interact with a wide variety of people both in LCCI and the US, at varying levels of the business. The role will report to Manager-CLS at LCCI.

Key Objectives/Deliverables:

Medical Writing (Content Development)

Partners with learning consultants and business partners to effectively gather and evaluate source content from multiple sources. Plans (including organizing/preparing outlines), write (including first-draft authoring), edit, review, and coordinate the creation of medical learning content (storyboard) Ensures that key content, scientific concepts, elements from internal guidance and resource documents are included appropriately in all learning content, and that all documents are well written, usable/executable, and compliant with policies and procedures. Ensures proper documentation of needed references and attribution of source material. Ensures and coordinates quality checks for accuracy, collate reviewer's comments, adjust content of training as required based on internal/external input, and prepare final version. Drives quality standards through review of project documents, design, deliverables, final learning content and evaluation data.

Project and Stakeholder management

Lead the writing process and apply effective project management skills to ensure timely completion of high-quality regulatory documents. Effectively manage multiple projects and exhibit flexibility in moving across therapeutic areas, and products, depending on project assignment. Builds, communicates, and manages credible project timelines. Influences or negotiates changes of timelines and content with other team members. Anticipates and mitigates risks to delivery. Anticipates and resolves project/program issues, escalating as appropriate.

Knowledge Sharing and Development

Maintains and enhances therapeutic area knowledge including disease state and compound(s) for assigned project(s). Maintains and enhances the medial writing skills to align with the audience needs and with the changes in technology and platforms. Provides coaching to others by sharing technical information, giving guidance, answering questions. Networks with others (including other functions and regions) to identify and share best practices. Contributes to process improvements, suggesting opportunities where appropriate.

Basic Requirements:

Demonstrated experience in technical scientific or medical writing. Demonstrated excellence with program/project management and time management skills. Demonstrated ability to establish strong business relationships. Ability to work independently and in a team environment. Demonstrated ability in conflict resolution, judgment and managing complexity. Ability to prioritize work and balance multiple projects simultaneously. Strong work ethic, personal motivation, and team player who is dynamic and result oriented Good presentation skills, interpersonal and communication skills, fluent (verbal and written) in English. Ability to operate effectively in an international matrix environment, with ability to work across time zones.

Additional Preferences:

Experience writing regulatory, clinical trial documents, publications and/or writing deliverables for Medical Affairs communications (slide decks, patient, or HCP materials, etc.). Experience working in a regulated environment. Experience working with US organizations. Strong organizational skills. Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates).

Education Requirements:

Bachelor's degree in a scientific, health, communications, technology health related field

Other Information:

Travel may be required.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

#WeAreLilly

  • Senior Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Quanticate Full time

    Quanticate is seeking a talented and experienced Senior Medical Writer to join our Medical Writing team in India. As a leading global clinical research organization, Quanticate works with pharmaceutical, biotechnology, and medical device companies to support their regulatory and scientific communication needs. The Senior Medical Writer will be responsible...

  • Senior medical writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk AS Full time

    Department - Clinical Reporting GBSWe are currently seeking a Senior Medical Writer to join the Clinical Reporting unit located in the Global Business Service (GBS) in Bangalore, India. Are you someone who thrives on challenges and excels in a dynamic work environment? Do you enjoy closely collaborating with key stakeholders and ensuring strategic alignment?...

  • Senior medical writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Department – Clinical Reporting GBS We are looking for a Senior Medical Writer in the Clinical Reporting unit based out of Global Business Service (GBS), Bangalore, India. Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic...

  • Senior Medical Writer

    1 week ago

    Bengaluru, Karnataka, India MIMS Pte Ltd Full time

    Job Overview:The Senior Medical Writer is responsible for providing scientific consultancy and creating high quality content for MIMS Med Comms tailored solutions to address the medical communications objectives of our client partners (e.g.Pharmaceutical, governmental, or healthcare providers)Key responsibilities of this position include:Maintain a deep...

  • Senior medical writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    The position The key responsibilities in this position will be to perform medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to the preparation of Protocols, Clinical Trial Reports (CTRs), Non-interventional study reports (NSRs), Layperson Summary (LPS), Investigator Brochure (IB), Regulatory...

  • Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk AS Full time

    Department – Clinical Reporting Unit Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might have...

  • Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk AS Full time

    Department – Clinical Reporting Unit Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might have...

  • Medical Writer 2

    1 week ago

    Bengaluru, Karnataka, India Novasyte Full time

    Job OverviewActs as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports, protocols, more challenging indications, or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the agreed timelines. May provide feedback to peers when asked...

  • Sr Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Thermo Fisher Scientific Full time

    Senior Medical Writer (India) (FSP) At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals...

  • Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Medical WriterCategory:Clinical DevelopmentLocation:Bangalore, Karnataka, INDepartment - Clinical Reporting UnitAbout the department**- The Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community in a short span of 6-7 years, since its inception in 2011. The team is a...

  • Senior Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Molecular Connections Full time

    Requirement Details.Job Description:Job Title: Medical WriterJob description:Prepare, review, and edit reports, manuscripts, drug monographs, medico-marketing material, systematic reviews, and meta-analysis on varied disease domainsPrepare, review, and edit reports on disease background, epidemiology, outcomes and disease burden in oncology and non-oncology...

  • Global Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    .Department - Global Medical Affairs. Are you a proven leader who can set direction and drive team performance? Do you have expertise in driving medical affairs strategy and tactics across therapeutic areas with a focus on diabetes, obesity and cardiometabolic portfolio? Then we might have the right position for you. We are looking for a Global Medical...

  • Junior Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Healthminds Consulting Full time

    Position:Junior Medical Writer:Education qualification: Masters in Life Science/Dental/Pharma and has knowledge of publicationsExperience: 1 year minimum in content development highly desiredSkills: Ability to summarize content from published literature in a concise and meaningful manner, relevant to objectives provided by client. Develop content with...

  • Safety Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Novo Nordisk Full time

    Department - GS GBS Safety Medical WritingThe PositionAs a Safety Medical Writer (SMW), you will plan, drive and co-ordinate preparation of safety documents to ensure submission according to agreed timelines. You will prepare aggregate safety reports, clinical risk management plans and responses to questions from health authorities in collaboration with...

  • Medical Communications Writer

    1 week ago

    Bengaluru, Karnataka, India Tag India Private Limited (TN State) Full time

    Key Responsibilities : 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...

  • Expert Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Merck Full time

    Work Your Magic with usReady to explore, break barriers, and discover more? We know you've got big plans - so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of...

  • Senior Medical Writer

    1 week ago

    Bengaluru, Karnataka, India Lifelancer Full time

    About the job At ICON, its our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our Own It culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability Delivery,...

  • Senior Tech Writer

    1 week ago

    Bengaluru, Karnataka, India Cloud Software Group Full time

    Senior Technical Writer (IC3) What we are looking for: The Cloud Software Group Information Development team invites candidates to apply for a Senior Technical Writer post, associated with producing technical content for its various products. A Senior Technical Writer is responsible for producing customer-facing product documentation using Agile...

  • Senior Technical Writer

    1 week ago

    Bengaluru, Karnataka, India SecPod Full time

    Senior Technical Documentation Writer at SecPod CareersWe are looking for an experienced Senior Technical Documentation Writer with 5–8 years of expertise to join our team at SecPod Careers. As a vital member of our team, you will be tasked with creating comprehensive, clear, and top-notch documentation for our software products, primarily focusing on...

  • Senior Technical Writer

    1 week ago

    Bengaluru, Karnataka, India SecPod Full time

    Job Description:We are seeking a skilled Senior Technical Documentation Writer with 5–8 years of experience to join our team. In this role, you will be responsible for creating comprehensive, clear, and high-quality documentation for our software products, with a focus on SaaS-based solutions. Your work will be instrumental in enabling our customers to...