Sr. Director - GRA, Global Regulatory Policy & Strategy - Oncology
Location: Indianapolis
Posted on: June 23, 2025
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Job Description:
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. Purpose: Global Regulatory
Policy & Strategy strives to enable Lilly to deliver innovative
regulatory results by identifying policy hurdles and emerging
trends, developing advocacy plans built upon science-based
positions, engaging broad partner networks, and ultimately
effecting change in regulatory policies that advance patient
outcomes, reduce regulatory risk, and improve efficiency in drug
development. The purpose of the Sr. Director – GRA Global
Regulatory Policy & Strategy - Oncology role is to elicit, develop,
and progress Lilly’s Oncology regulatory policy positions and
related advocacy strategies to enable innovation and ultimately
improve outcomes for patients. In this role, you will represent
Lilly in external consortia and policy-related forums and rely on a
strong pre-existing network of external collaborators. Primary
Responsibilities: Establish Regulatory Policy Positions and
External Engagement Strategies Gain consensus on Lilly’s priority
global regulatory topics consistent with GRA’s overall regulatory
policy vision, which will center around topics that encourage
innovation in drug development and regulatory review of medicines
targeting various types of cancers. Critically review and analyze
regulatory and legislative proposals and identify possible policy,
political, and financial impact to Lilly in cooperation with
cross-functional partners Articulate regulatory policy challenges,
problem statements and desired future states. Identify and develop
data and evidence to support company positions, working in
collaboration with cross-functional colleagues. Bring in or
represent external viewpoints as company positions are developed.
Cultivate relationships and collaborate with internal subject
matter authorities, including Oncology colleagues and regulatory
team members, among others, to create evidence and positions. Build
and implement tactical policy plan. Exert External Influence Engage
on behalf of Lilly in health-policy related forums. Triage
opportunities to engage externally so that the appropriate company
experts can contribute. Attend and present at key industry
conferences to showcase Lilly policy positions. Build upon existing
relationships and maintain strong collaborations with external
patient/professional groups, think-tanks, academic groups, policy
organizations and trade associations. Impact patient outcomes
through collaboration across partner groups Effectively lead,
engage and partner Exemplify Team Lilly behaviors: Include,
Innovate, Accelerate, Deliver in internal and external
interactions. Model the innovation and leadership behaviors and
regulatory excellence attributes as described in Global Regulatory
Affairs white papers. Engage in forums that share regulatory
information across GRA components and other Lilly teams and
business partners. Create and lead in an environment that
encourages open discussions on issues to achieve a robust outcome
on business decisions. Minimum Qualification Requirements: Masters’
degree or Doctorate in relevant policy, public health, regulatory,
clinical, legal, business, research, or related field with 5 years
regulatory/policy/advocacy equivalent experience OR Bachelor’s
degree with 10 years regulatory/policy/advocacy equivalent
experience Experience engaging in external consortia. Established
external network in oncology policy. Recognized experience in
leading/implementing public policy or regulatory policy campaigns.
Additional Skills and Preferences Passionate about crafting policy
solutions. Previous experience shaping regulatory policy issues
related to oncology. Prior work with organizations such as Friends
of Cancer Research, LUNGevity, or Cancer Support Community
Proficient in researching and writing briefings, positions, and
high-level communications for executive staffing. Ability to
influence without authority, demonstrate resourcefulness, and
operate independently. Additional Information: Travel up to 20%
Position Location – Indianapolis, IN, Washington DC or Remote 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 proud to be an
EEO Employer and does not discriminate on the basis of age, race,
color, religion, gender identity, sex, gender expression, sexual
orientation, genetic information, ancestry, 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 are open to all employees.
Our current groups include: Africa, Middle East, Central Asia
Network, Black Employees at Lilly, Chinese Culture Network,
Japanese International Leadership Network (JILN), Lilly India
Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ
Allies), Veterans Leadership Network (VLN), Women’s Initiative for
Leading at Lilly (WILL), enAble (for people with disabilities).
Learn more about all of our groups. Actual compensation will depend
on a candidate’s education, experience, skills, and geographic
location. The anticipated wage for this position is $177,750 -
$260,700 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).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. WeAreLilly
Keywords: , Indianapolis , Sr. Director - GRA, Global Regulatory Policy & Strategy - Oncology, Science, Research & Development , Indianapolis, Indiana