CMCPM Radiopharmaceuticals

BioSpace

Indianapolis (IN)

Hybrid

USD 151,500 - 222,200

Full time

14 days+

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Benefits offered by this job

Comprehensive benefits

401(k) with company match

Company bonus potential

Job summary

A global healthcare leader is seeking a Director for CMCPM Radiopharmaceuticals in Indianapolis. The role involves leading the creation and implementation of CMC plans, collaborating with global program teams to drive CMC development and delivery goals. Candidates should have over 10 years of relevant experience and a four-year degree in a scientific or engineering field. The position offers a dynamic work environment with remote or onsite options, competitive compensation, and comprehensive benefits.

Qualifications

10+ years of drug development or radiopharmaceutical product experience.
Practical experience leading cross-functional projects, preferably within radiopharmaceutical CMC.
Demonstrated ability to communicate complex issues accurately.

Responsibilities

Partner with global program teams to translate strategy into CMC development goals.
Lead creation and implementation of integrated CMC plans.
Drive cross-functional CMC teams to maximize the value of data.

Skills

Drug development experience

Project management tools

Cross-functional leadership

Communication skills

Education

Four-year degree in a scientific or engineering field

Job description

CMCPM Radiopharmaceuticals

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.

Organizational Overview

CMC Project Management is responsible for leading the creation, development, communication and implementation of integrated CMC plans for assets from portfolio entry to global submissions/approvals and launch. The position provides strategic and operational leadership to CMC and global product teams, co‑leading the cross‑functional team in partnership with technical leaders and department heads, who are accountable for technical deliverables.

Key Responsibilities

Effectively partner with global program teams and therapeutic business units to translate preclinical, clinical, and asset strategy into CMC development & delivery goals (working closely with asset leadership, PPM, clinical/medical, and regulatory partners).
Lead the creation, development, communication and implementation of integrated CMC plans for assets from portfolio entry through early‑phase clinical development (inclusive of both therapeutics and imaging agents).
Leverage portfolio knowledge, development and financial acumen to enable investment strategies and optimization at both project and portfolio level.
Drive cross‑functional CMC teams to maximize the value of data, create bold, competitive plans, anticipate risks, effectively communicate risks, enable high quality decisions at fast speed and implement decisions.
Understand when and how to appropriately raise issues to teams and to stakeholders. Keep both team members and stakeholders fully apprised of project status and issues at the right level of detail.
Develop high performing matrix teams with an ability to quickly identify gaps in team effectiveness and implement remediation efforts to ensure project success.
Support Due Diligence efforts by leading CMC development plans while integrating and communicating key findings with stakeholders.
Participate in or lead continuous improvement projects, which significantly impact the work and/or effectiveness of CMC development.

Required Experience and Skills

10+ years of drug development or radiopharmaceutical product experience.
Four‑year degree, preferably in a scientific or engineering field.
Practical experience leading cross‑functional projects, preferably within radiopharmaceutical CMC.
Demonstrated expertise in PM tools and processes (e.g. management of scope, timeline, cost, communications, risk and procurement as defined by PMBOK), with ability to identify and drive business process improvements and incorporate new PM technologies/methodologies.
Demonstrated ability to communicate complex issues accurately and succinctly, both horizontally and vertically across the development organization.

Preferred Skills and Experiences

Advanced degree (Master of Science, Master of Business Administration, Ph.D. or PharmD.).
Understanding of development phases, associated radiopharmaceutical CMC deliverables, and interactions of various functional areas and how each relates to a comprehensive development strategy.
Experience in clinically‑enabling radiopharmaceutical CMC development, inclusive of therapeutics and imaging.
Understanding of early‑ & late‑phase therapeutic landscapes, incl. clinical & regulatory environments.

Physical Demands/Work Environment

The physical demands of this position are consistent with light office duties, performed in a typical office setting.

Location

Remote or onsite

Accommodations and EEO Statement

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.

Compensation and Benefits

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $151,500 - $222,200. Full‑time equivalent employees will also 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.

Job Details