Recruitment Data Policies Medical Strategy Lead Regenerative Neural Cell Therapy

Make your mark for patients

We are looking for an exceptional Medical Strategy Leadwho is strategic collaborative and scientifically credible to join our United States Medical team based out of our US Headquarters in Smyrna GA.

About the role

You will be responsible for the planning and implementation of pre-launch launch and lifecycle medical strategies for Rezanecel in alignment with the global medical development strategy. You will also advise on US field medical engagement and represent the US field medical perspective within the Global Rezancel Medical Team .

Who youll work with

You will partner closely with the global asset medical team and colleagues across Clinical Development Evidence Generation Patient Safety Market Access Marketing Legal and Compliance. You will also guide United States field medical colleagues and engage external scientific experts investigators professional associations treatment centers payer stakeholders and patient organizations.

What youll do

• Lead United States medical strategy launch readiness and lifecycle planning aligned globally

• Translate clinical-development priorities into compliant field medical plans resources and scientific messaging

• Coordinate medical readiness across planned clinical sites with development and study-operations partners

• Oversee medically sound content data dissemination publications and contextualized scientific information

• Build trusted relationships with scientific experts researchers professional bodies and patient organizations

• Define objectives and measures for execution quality insights stakeholder impact and effectiveness

Interested For this role were looking for the following:

Minimum requirements

• Doctoral degree (MD/PhD) in medicine or science with neurology or epilepsy expertise

• 8 years of pharmaceutical or biopharmaceutical medical-affairs experience

• 3 years leading medical strategy within a matrix organization

• 3 years supporting drug development and regulatory approval processes

• Demonstrated success translating scientific and clinical strategy into effective field execution

• Credibility with United States scientific experts professional societies and neurology treatment centers

Preferred requirements

• Have led the launch of a novel therapy or significant shift in treatment practice

• Familiarity with United States regulatory interactions and reviewer engagement

• Proven ability to derive actionable insights from scientific stakeholder engagement

• Strong track record influencing cross-functional teams in a matrix environment

• Skilled in developing medical resources scientific messaging and launch-enabling tools

• Demonstrated success using metrics to evaluate medical impact and operational effectiveness.

Salary

The reasonably anticipated salary range for this position is $236800 to $310800 per year. The actual salary offered will take into account related knowledge skills experience and location among other factors and may fall outside the expected range.

Are you ready to go beyond to create value and make your mark for patients If this sounds like you then we would love to hear from you!

About us
UCB is a global biopharmaceutical company focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe inspired by patients and driven by science.

Why work with us
At UCB we dont just complete tasks we create value. We arent afraid to push forward collaborate and innovate to make our mark for patients. We have a caring supportive culture where everyone feels included respected and has equal opportunities to do their best work. We go beyond to create value for our patients and always with a human focus whether thats on our patients our employees or our planet. Working for us you will discover a place where you can grow and have the freedom to carve your own career path to achieve your full potential.

At UCB weve embraced a hybrid-first approach to work bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employment decisions will be made without regard to any characteristic protected by applicable federal state or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment your employment with UCB or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws orders and regulations.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.