Associate Manager Medical Writing

Associate Manager Medical Writing #medicalwriting #medicalcommunications #medcomms #medicalwriter #healthcarecommunications #medicalwriters #medicalwritingtips #agencylife #medcommsjobs #wearewe #scientificservices #medcommsagency #medicalwriterlife #medcommsrecruitment #medcommscareers #medicalwritingservice #scientificdirector #seniormedicalwriter #medical #medcommslife #principalmedicalwriter #editorialteamlead #clinicaltrials #principalwriter #medicine #healthcare #pharmacovigilance #clinicalresearch #pharmacy #medicaleducation At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring lifechanging medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We re looking for people who are determined to make life better for people around the world. Position Description: The Medical writer is responsible to help LMI CLS to create medically related content in support of product, disease state, clinical trial, and marketplace material for the marketing and sales organizations. This includes creation revisions, coordination, and implementation of learning content for product trainings across sales and marketing both at Global and affiliate level including, but not limited to, creating updating wireframes, building reference packages, creating updating training modules. The CLS 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. The CLS Medical Writer ensures quality design and content development of product related training 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 LMI Team Leader at LCCI. Key ObjectivesDeliverables: Medical Writing Content Development Partner with learning consultants, content developers and business partners to effectively gather, evaluate and leverage source content from multiple sources Partner with Content Developer to plan including organizingpreparing outlines, write, edit, review, and coordinate the creation of medical content wireframe for all product related trainings Ensure that the content is within the right context, flow, and relevant medical information knowledge Ensure that key content, scientific concepts, elements from internal guidance and resource documents are included appropriately in all training documents Ensure that all documents are well written, usableexecutable compliant with policies, procedures, and external regulatory requirements including medical, legal, and regulatory requirements Ensure proper documentation of needed references and attribution of source material. Ensure and coordinate quality checks for accuracy, collate reviewer s comments, adjust content of training as required based on internalexternal input, and prepare final version Drives quality standards through medical review of project documents, deliverables, final learning content and evaluation exams and knowledge assessments data Project and Stakeholder management Lead the medical writing process and apply effective project management skills to ensure timely completion of highquality training documents Effectively manage multiple projects and exhibit flexibility in moving across therapeutic areas, and products, depending on project assignment Contribute towards building, communicating, and managing project timelines Influence or negotiate timeline and content changes with other team members. Anticipate and mitigate risks to delivery Effectively collaborate and work with teams and stakeholders including Brand team medical, legal, and regulatory personnel to ensure smooth and timely project completion and escalate issues, as appropriate. Knowledge Sharing and Development Maintain and enhance therapeutic area knowledge including disease state and compounds for assigned projects. Maintain and enhance the medial writing skills to align with the audience needs and with the changes in technology and platforms Provide coaching to others by sharing technical information, giving guidance, answering questions Network with others including other functions and regions to identify and share best practices. Contribute to process improvements, suggesting opportunities where appropriate Basic Requirements: Demonstrated experience in technical medical scientific writing 24 years of experience in medical scientific writing Demonstrated excellence with programproject management and time management skills. Successful completion of a writing exercise. Demonstrated ability to establish strong business relationships. Ability to work independently and in a team environment Experience working with US organizations Demonstrated ability in conflict resolution, judgment and managing complexity. 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 working in a regulated environment Strong organizational skills Experience writing regulatory, disease state, clinical trials, marketplace, Prescribing Information related documents andor writing deliverables for Medical Affairs communications slide decks, patient, or HCP materials, etc. Demonstrated highlevel enduser computer skills e.g., word processing, tables and graphics, spreadsheets, presentation, and templates Education Requirements: MAMSc degree in a scientific, health, communications, technology health related field Other Information: Travel may be required. Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries collectively Lilly are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources Lilly_Recruiting_Compliancelists.lilly.com for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response. 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.