Associate/Manager - Regulatory Project Management and Operations
US: USA Remote
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.
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.
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
Akouos, Inc. a wholly owned subsidiary of Eli Lilly and Company, is a leading precision genetic medicine company focused on inner ear disorder. We are developing targeted Adeno-Associated Viral (AAV) vector-based gene therapies for sensorineural hearing loss, the most common form of hearing loss and one of the most common of all sensory disorders
The Manager, Regulatory Operations and Project Management will be responsible for supporting Regulatory Leads and cross-functional program teams in the preparation and maintenance of global regulatory submissions. This individual will also play a pivotal role in the implementation of regulatory systems and processes to support regulatory process improvement.
Responsibilities:
- Manage the preparation and maintenance of global regulatory submissions in partnership with Regulatory Leads and cross-functional teams
- Effectively monitor and communicate the progress of regulatory projects to relevant stakeholders
- Support the authoring of regulatory dossier documents with guidance from Regulatory Leads
- Implement and oversee systems for maintaining and tracking regulatory information, including archives of regulatory submissions, correspondence, and commitments
- Proactively develop solutions to remove barriers and maintain project deliverables
Basic Requirements:
- Bachelor’s Degree in life science or related scientific discipline
- 1-3+ years of related work experience in regulatory affairs, regulatory operations, and/or project management
Additional Skills/Preferences:
- Excellent organizational, communication, and project management skills
- Demonstrated ability to work well in a collaborative and dynamic team environment, set priorities, and drive results
- Highly proficient in Microsoft and project management applications
- Working knowledge of eCTD publishing systems, regulatory/document management systems, and related tools
- Previous eCTD filing experience and a clear understanding of global regulatory submission content and format requirements, as well as the interdependencies between submission components
- Excellent document drafting, editing, and proofreading skills, with high attention to detail
- A collaborative team player with a "can do" attitude and an eagerness to grow and apply their regulatory knowledge
Additional Information:
- Some travel as needed for conferences, regulatory and/or policy meetings, and other professional development opportunities.
- USA Remote
- Full time
- Lilly currently anticipates that the base salary for this position could range from between $61,500 to $143,000 and will depend, in part, on the successful candidate’s qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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 is an EEO/Affirmative Action Employer and 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.
Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
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Flexible benefits Vacation Vacation benefits Volunteerism
Tasks- Implement regulatory systems
- Manage regulatory submissions
- Monitor project progress
- Regulatory submissions
- Support regulatory document authoring
Attention to detail Communication Document management systems ECTD publishing systems Healthcare Leadership Microsoft Applications Organization Organizational Philanthropy Process Improvement Project Management Proofreading Regulatory Affairs Regulatory management systems Regulatory Submissions Volunteerism
Experience1-3 years
EducationBachelor's degree DO Life Science Scientific discipline
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9