Job
Description
Summary
Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements Ensures compliance to the requirements from regulatory agencies Maintains the technical and non-technical documentation change system Assures procedures are in place to classify and maintain records Interprets and enforces all documentation formatting, standards, policies, and operating procedure requirements May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched May maintain extensive knowledge of product information and continuous contacts with local, regional, and divisional customers, About The Role Key Responsibilities Structured Data Submissions (SDS): Independently perform timely SDS ( e-g xEVMPD, IDMP) via RIM system, ensuring data quality and exchange with EMA including analysis and tracking of 3rd acknowledgements Ensure Data Quality Management and timely delivery of requests for new/changes of code lists/terms including external reference data ( e-g SPOR), Provide guidance and support to cross-functional teams related to planning, submission compilation and dispatch of worldwide compliant SDS, as well as submission filing strategy, eCTD document lifecycle management and workflows, in alignment with FHIR (Fast Healthcare Interoperability Resources) Assess SDS resources and support needs and develop/implement solutions to create efficiencies Effectively troubleshoot technical/quality issues relating to compilation, validation and dispatch of global submission outputs, Coding of Clinical Particulars: Perform coding of the Clinical Particulars attributes in Novartis Regulatory Information Management (RIM) system: Therapeutic Indications and Co-morbidity using the MedDRA dictionary, Intended effect using a controlled vocabulary, as required to ensure compliance with xEVMPD / IDMP requirements, Review and maintain MedDRA code values used in EU registrations upon MedDRA version updates by performing gap analysis of changes, and update existing values accordingly in RIM system Review and update coding values as needed upon queries from the European Medicines Agency (EMA), for instance receipt of 3rd acknowledgment, Interactions: Liaise with GDD colleagues regarding new regulatory requirements and related business processes, to ensure proper knowledge transfer to IT business partners for system enhancement requests, Manage interactions and collaboration with RA Country Organisations (CO), Global RA and non-RA functions on regulatory and compliance maintenance activities for Authorised and Investigational medicinal products, Optimally support QPPV and PV-related processes (incl fees), provide support for internal /external audits /inspections Facilitate and/or participate in meetings with internal and external stakeholders (including acquisitions, partnerships and divestiture efforts) Participate as key business contributor in Technology initiatives including, but not limited to, systems upgrades, validation, implementation activities and functionality enhancements, including external service providers, General & Training: Support user training of RA end users, as required, Coach / mentor new team members Support PQ testing and Application verification activities, as required Support preparation of administrative procedures and Working Instructions to support system implementations Develop, implement, and support innovative regulatory strategies and life-cycle management of RA systems, including process productivity and efficiency improvement and propose potential solutions Identify and investigate operational needs, problems, and opportunities, contribute to the implementation of improvements within area of responsibility, Minimum Requirements BS in Life Sciences (Medicines/Pharmacy) or a relevant discipline with at least 7 years of professional work experience Masters degree preferred (M Pharma or MD), 4-6 years of relevant experience in structured data submissions ( e-g xEVMPD) and use of RIM systems, including familiarity with submission publishing activities, 3-5 years in Clinical coding ( e-g MedDRA, SNOMED), Labelling, Regulatory Affairs or Regulatory submission related experience WITH SDS experience as 1st bullet, Proficient knowledge of EMAs databases ( e-g SPOR), Knowledge and experience with eCTD, xEVMPD, IDMP, Publishing Standards and applicable related tools is desirable, Experienced in using RA systems of data (RIMS, DMS, Change Control databases), systemsdata model and vocabularies Familiar with the drug development and registration process, Solid project management, organizational and time management skills to manage multiple ongoing projects simultaneously, Familiar with global Health Authority regulations/guidelines e-g , FDA regulations, ICH and EMA guidelines/directives, Proficiency with computer programs/systems (MS office, etc) with demonstrated ability to learn new systems quickly Strong analytical skills and problem-solving skills Ability to coordinate and work effectively with cross-functional teams Why Novartis: Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world How can we achieve thisWith our people It is our associates that drive us each day to reach our ambitions Be a part of this mission and join us! Learn more here: https:// novartis / about / strategy / people-and-culture Youll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook https:// novartis /careers/benefits-rewards Commitment To Diversity And Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve, Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl india@novartis and let us know the nature of your request and your contact information Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork novartis /network Why Novartis: Helping people with disease and their families takes more than innovative science It takes a community of smart, passionate people like you Collaborating, supporting and inspiring each other Combining to achieve breakthroughs that change patientslives Ready to create a brighter future togetherhttps:// novartis / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for youSign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork novartis /network Benefits and Rewards: Read our handbook to learn about all the ways well help you thrive personally and professionally: https:// novartis /careers/benefits-rewards Show
