Publication Planning Associate – VEO publications in Bangalore

Job Description

Join American pharmaceutical leader Eli Lilly and Company, currently hiring Publication Planning Associate – VEO publications in Bangalore, Apply Lilly careers in Bangalore Karnataka.


Position : Publication Planning Associate – VEO publications

Location : Bengaluru, India

Job id: R-32758


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:Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.The purpose of the Publication Planning Associate – LCCI VEO role is to manage the implementation of all Publication plan(s) for VEO publications.The Publication Planning Associate – LCCI VEO is responsible for managing and tracking all VEO Publication plans and tactics across all assets. Publications include abstract presentations for scientific meetings, peer-reviewed journal articles, review articles, and other publication related deliverables. The Publication Planning Associate – LCCI VEO serves as apoint person for all units within Lilly that contribute to, or are affected by, VEO publication development. Additionally, the Publication Planning Associate – LCCI VEO is responsible for facilitating publication team meetings, providing status metrics to the team and leadership, and managing other materials to meet the publication teams’ needs, ensuring thatdeadlines for publication submission are met and change control and project budget(s) are monitored/managed.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 jobresponsibilities and any related duties that may be required for the position.1. Scientific Disclosure Plan Management• Provides expertise on VEO publication planning strategy and tactics• Manages and executes the VEO publication plan tactics based upon strategy• Manages implementation for all VEO publications across all compounds• Works with all Publication Strategy Leads and all other Publication Planning Associates across all compounds to execute on the VEO publication plans• Works with all VEO scientists and project managers across all compounds to execute on the VEO publication plans• Develops and maintains publications metrics/dashboard for all VEO compounds. Seeks business partner feedback updates as applicable• Ensures that VEO publications budgets for projects are met• Organizes content for and leads VEO publications strategy and operational meetings, including change controls, escalations and project updates• Responsible for content for VEO Publication Plan–related slide decks detailing strategy, progress and metrics• Collaborates with all GSC Publication Specialists to ensure publication tracking tools are up to date with accurate information• Works with internal and external authors and publication vendors on timelines and process• Ensures disclosures are aligned to appropriate venues and methods of disclosing study results in a manner that is compliant with PhRMA and ICMJE guidelines as well as Eli Lilly policy• Identifies, evaluates, and resolves conflict across GSC and VEO teams. Elevates those that require input from senior management• Ensures that VEO publications achieve the balance between business needs, scientific integrity, and compliance with publication guidelines2. Publication Deliverable Oversight• Survey and gather supporting literature, analyze tables and listings, and formulate graphics to represent dataappropriately in VEO publications• Appraises and critically evaluates VEO scientific literature and data• Ensure quality reviews and edits of publications occur• Lead the coordination of VEO scientific congress deliverables and ensure consistency within and across assets• Functions as the expert on VEO Lilly disclosures at scientific congresses• Ensures SOPs are well understood across the team and affiliate(s), leading and providing clarification on local implementation3. Subject Matter Expert• Maintain and enhance expert knowledge on industry guidelines pertaining to data dissemination (e.g., CONSORT, ICMJE, GPPs) and interactions with health care providers (e.g.PhRMA Code, AdvaMed guidelines)• Maintain and enhance expert knowledge of Lilly and GSC publications processes, and relevant VEO processes• Exhibit flexibility in moving across document types, therapeutic areas, and compounds, in supporting all VEO compound publication plans• Advocate for innovative advances in addressing audience needs and with the changes in technology and platforms• Lead and advocate for potential process improvements• Responsible for capturing and tracking new ideas that may lead to improvements in process• Coach and share learnings, and ensure consistency across all compounds in VEO.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▪ Excellent communication (written and verbal) and interpersonal skills▪ 3 years experience in project management with demonstrated ability to lead projects, manage timelines, and providesuccinct progress updates to teams and leadershipOther Information/Additional Preferences:▪ Graduate degree with formal research component or in life sciences.▪ Knowledge of scientific principles, research design, data interpretation, manuscript composition, and Good Publication Practices▪ Previous project leadership▪ Experience in clinical development, clinical trial process or regulatory activities▪ Experience in health outcomes, economics, real world evidence▪ Capable of managing multiple projects simultaneously and re-evaluating priorities as appropriate▪ Good organizational, project management, business, and communication skills▪ Familiarity with Good Publication Practices, ICMJE requirements, and PhRMA guidelines▪ Experience managing project budgets▪ Located at Lilly Capability Center India, Bangalore▪ Ability to travel: Up to 20%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 ( ) 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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