Associate / Senior Associate – Global Scientific Communication – Health Literacy Content Creation in Cork

Job Description

Join American pharmaceutical leader Eli Lilly and Company, currently hiring Associate / Senior Associate – Global Scientific Communication – Health Literacy Content Creation in Cork, Apply Lilly careers in Cork Cork.

 

Position : Associate / Senior Associate – Global Scientific Communication – Health Literacy Content Creation

Location : Cork, Ireland

Job id: R-27164

 

Job Details

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 35,000 employees around the world work to discover and bring life-changing 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.Purpose:  To improve patient experiences throughout the clinical trial lifecycle, Lilly is creating a new, leading-edge internal health literacy capability. This innovative team will be tasked with creating dynamic, patient-facing clinical trial communications in the realms of patient education, recruitment, retention, proactively executing fully coordinated health literacy optimized content strategies.  The purpose of the Associate / Senior Associate – Global Scientific Communication – Health Literacy Content Creation role is to work with cross-functional, multidisciplinary, therapeutic area molecule teams to prepare health literacy optimized clinical trial patient-facing communications.  Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.  1. Document Preparation, Development and Finalization/Document Management Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to effectively create and deliver impactful and streamlined health literacy optimized patient-facing clinical trial communications.  Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review and coordinate the publication and distribution of patient-facing clinical trial health  literate communications.  Conduct effective document initiation to ensure authoring team alignment, optimal audience engagement, base message and understanding.   Ensure data are presented in a clear, complete, accurate, and concise manner.  Ensure that key data, strategically aligned scientific narrative, elements from internal guidance and resource documents are included appropriately in all documents, and that data and content created is integrated, accurate, balanced and supported by appropriate data.  Ensure and coordinate quality checks for accuracy, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version.   Exhibit flexibility in moving across development and preparation of multiple document types.   Work with Health Literacy team and extended teams to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.  Leverage health literacy best practices to ensure all content is optimized for intended audiences.  Influence or negotiate change of timelines and content with other team members. Adhere to compliance standards leveraging the Lilly Brand book and Lilly Global Health Literacy Toolkit  Advocate internally and externally for appropriate audience engagement and best health literacy practices on all applicable work products.  Work with internal and external speakers or with vendors as needed, to develop and prepare presentations. 3. Project and Stakeholder Management  Lead the writing process and apply effective project management skills to ensure timely completion of documents Serve as the BU health literacy content creation point of contact for molecule teams to offer best practices and creative strategies to create dynamic content experiences 4. Knowledge and Skills Development  Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s).  Maintain and enhance content creation skills to align with audience needs and technology/digital evolution  Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment.  5. Knowledge Sharing  Provide peer coaching to others by sharing technical information, giving guidance, answering questions.   Recognized for technical expertise in  development of health literate documents.   Network with others (including other functions and regions) to identify and share best practices.  Contribute to process improvements, suggesting opportunities where appropriate. Minimum Qualification Requirements:    Bachelor’s degree in scientific, health, communications, or technology related field  Or, Bachelor’s degree in any field with at least two years of clinical development experience  Strong communication and interpersonal skills A writing exercise is required as part of the candidate evaluation process Other Information/Additional Preferences:   Advanced degree (PhD, MD, PharmD, MA, MBBS) in sciences or health related field. Experience in health literacy, patient-facing communications  Experience in working with medical professionals Demonstrated mastery of verbal and written English skills in the medical, scientific or health outcomes or technical  writing fields Previous training and experience in disseminating results in clinical, health economics, health outcomes, health literacy, disease management, and/or population health. Experience in medical writing  Relevant experience in clinical development, clinical trial process, health-outcomes research or regulatory activities  Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise).  Demonstrated project management and time management skills. Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates). Extensive experience in writing, reviewing, and publishing scientific materials and the ability to appraise scientific literature and raw data critically. Ability to communicate clearly and succinctly with all audiences and forums through exemplary oral and written communication skills. 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_Compliance@lists.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.

 

 

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