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 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.

Eli Lilly Cork is made up of a talented diverse team of over 2000 employees across 60 nationalities who deliver innovative solutions that add value across a variety of Business Service functions including Finance, Information Technology, Medical, Clinical Trials and more. Eli Lilly Cork offers a premium workspace across our campus in Little Island, complete with flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies and on-site parking. Inhouse People Development services, Educational Assistance, and our ‘Live Your BEST Life’

wellbeing initiatives are just some of the holistic benefits that enhance the career experience for our colleagues.

Eli Lilly Cork is committed to diversity, equity and inclusion (DEI). We cater for all dimensions ensuring inclusion of all ethnicities, nationalities, cultural backgrounds, generations, sexuality, visible and invisible disabilities and gender, with four pillars: EnAble, embRACE, LGBTQ+ & Ally and GIN-Gender Inclusion Network. EnAble, our pillar for people with disabilities and those that care for them, partners with the Access Lilly initiative to make our physical and digital environment accessible and inclusive for all. Together they are committed to promoting awareness to create a disability confident culture both at Eli Lilly Cork and beyond.

Come join our team - Be Creative, Be an Innovator, and most of all, Be Yourself!

***12 month contract position***

Purpose:

The purpose of the Regulatory Delivery and Excellence (RD&E) Global Submission Publisher role is to:

execute and maintain global regulatory submissions from candidate selection through end of product lifecycle.
provide maintenance support as needed for submissions.
coordinate the creation and legalization of regulatory submission documents supporting registration activities across the international region
meet customer requirements by optimizing business processes, tools and ensuring implementation of the regulatory agency’s preferred electronic common technical document (eCTD) specifications in a quality way to promote timely review by the regulatory agency.
build eCTD and/or non-eCTD expertise and partner with Global Regulatory Associates, Regional Submission Associates, Affiliate Regulatory, other publishing centers, vendors, and/or other contributing areas to align on submission specific requirements and to ensure adherence to submission regulations and guidelines.

Although submission publishing work is technical, producing dossiers is a cross-functional process demanding an environment
of critical time frames and potentially changing priorities, and, therefore, a strong emphasis is placed on teamwork,
communication, and self-management.

Execute submission workload

Responsible for managing multiple submission types across assigned molecules.
- Coordinate and communicate with Regulatory Associates to execute planned compliance and strategic submissions.
- Proactively manage 30-day packets to ensure compliance.
Review and monitor the RIM or Share Point Calendar for delivery of planned documents in support of submissions and proactively update document status to manage workload and provide information on specific documents’ status as it pertains to any specific submission ensuring submissions are proactively processed such that they are delivered according to the planned submission date.
Escalate issues that may impact submissions and timelines.

Technical leadership for regulatory document legalizations

Coordinate/facilitate the creation of Authorization Letters, Power of Attorney letters, and other corporate administrative documentation to support registration activities, and develop/maintain related business process documentation
Coordinates apostille/legalization process for letters and certificates, as necessary Further develop and maintain archiving filing system
Collaborate with Regulatory scientists, regional and affiliate regulatory colleagues to streamline and improve the document legalization practices
Maintain transparent tracker of legalization activities and provide timely answers, advice, and document delivery to affiliates to meet the regulatory submission requirements
Communicate changes to tools, processes and procedures that directly affect the documentation activities
Stay current with the changing regulatory environment, new legalization requirements, and government standard practices
Ensure quality assurance and appropriate documentation of submission documents
Manage escalations in cases where urgent legalization is needed

Submit and archive registrations

Submit and archive submitted submissions, assuring all metadata fields are complete in RIM.
Manage FDA Web trader account to enable submissions via electronic gateway.
Assure all appropriate metadata fields are completed when archiving in electronic filing system (RIM).
Assure accurate entry for future retrieval of submissions if/when requested.

Build on high level of expertise in electronic publishing

Achieve a high level of technical and practical proficiency with RIM, Adobe Acrobat, Submission Validation software (Lorenz), ISIToolbox.
Successfully complete the formal training modules.
Stay up to date on system and tool upgrades that impact publishing.
Share technical information among staff members and apply what is learned in day-to-day work.
Apply learning from quality review of submission work.
Keep up to date in subject matter expert area.

Build technical and quality expertise

Understand changes to Regulatory Guidance and Requirements and advise RDE
Management as to their potential impact on Publishing.
Keep current on latest quality improvement methods.
Ensure best practices through partnership with Regulatory Quality.

Build Subject Matter Expertise within the Publishing Role and Process:

Oversight of QC process

Maintain QC process, checklists, and training materials.

Provide training for QC pool activities (those performing QC).
Ensure QC pool is aligned on process, interpretation of checklist items and QC feedback to publishers.
Provide technical leadership to QC personnel in resolving any QC issues or questions.
Assess needs and participate in skill enhancement exercises or opportunities.

Oversight of RIM Publishing Calendars

Monitor the RIM Submission Publishing calendar to ensure daily submission work is appropriately assigned and prioritized.
Serve as point of contact and subject matter expert for publishing calendars.

Technical leadership- for electronic publishing systems and process

Build and maintain high level of expertise in eCTD regulations and electronic publishing systems: eCTD XPress and accompanying tools.
Understand changes to Regulatory Guidance and Requirements and advise RDE Management as to their potential impact on tools, processes, procedures, publishing strategies and best practices with eCTD.
Provide technical leadership and timely answers to Submission Publishers on eCTD questions/issues to achieve a high level of technical and practical proficiency.
Provide feedback/training to business contributors and drive establishment of best practices and internal standards.
Create and maintain an open forum to discuss day to day publishing issues and drives implementation of any needed improvements or solutions.
Provide timely answers to requests from management, RAs, QC, and external parties regarding eCTD issues.

Partner with respective eCTD IT experts to ensure customer needs are understood for timely and validate solutions for routine system processes and tool updates.
Assist in end user testing where appropriate.

Training Assistant-Oversight of Submission Publishing Training program

Oversees the creation and management of submission publishing training materials.
Consults with the regulatory registrations process owner and subject matter experts on the content and delivery of training materials.
Responsible for ensuring that training processes for orientation of new resources are defined and maintained as submission processes evolve.
Provide guidance and coaching to those resources identified to assist in the delivery of training.

Asset Protection/Compliance

Ensure compliance with all Federal, State and Local guidelines to include Regulatory Agencies regulations and Lilly policies and procedures.

Minimum Qualification Requirements:

A minimum of 3-5 years in the biotechnology or pharmaceutical industry.
Experience with CTD/eCTD structure and format.
Experience using eCTD compliant publishing system
BS Degree in life science or computer science preferred or equivalent work experience.

Other Information/Additional Preferences:

The following skills and abilities are directly related to the essential functions of the job.

Three years of regulatory operations experience within a regulated environment with experience and knowledge in formatting and publishing medium/high complexity major applications, amendments, and supplements (manufacturing, nonclinical, clinical).
Experience with Original IND and supplemental MAA eCTD submissions including complex lifecycle submissions.
Experience with non-eCTD submissions including complex lifecycle submissions
Strong knowledge of global health authority and ICH regulations and guidance as it pertains to format and submission structure.
Current knowledge of CBER/CDER regulatory technical requirements

Computer Skills:

Proficiency with MS-Office Suite and Adobe Acrobat, including pdf plug-ins that support submission readiness
Experience with document management and Regulatory Information Management Systems (RIM)
Broad technical knowledge (MS Word, Adobe Acrobat PDF Bookmarks and Hyperlinks, Acrobat Plug-ins, Document Management Systems, Excel, ISI Toolbox, Lorenz)
The individual must be able to maintain the security of confidential information

Other Information:

This position reports functionally to a RDE publishing Manager.
This position is office-based work at Global Business Solutions Center (GBS) based at Cork, Ireland.
The shift for the position is Monday through Friday, 8 hours a day.
Some overtime may be required.

The statements contained in this document are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be an exhaustive list of all responsibilities, duties and skills of personnel so classified.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and 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.

#WeAreLillyUKandIreland

Associate / Senior AssociateGlobal Regulatory Affairs-Cork-Regulatory Delivery & Excellence-Global Publisher

Benefits

Job Description