Make your mark for patients

We are looking for a Regulatory Science Lead (Associate Director of Regulatory Affairs) who is a proactive, collaborative, and strategically minded individual to join us in our US Regulatory Affairs team, based in our Smyrna (Atlanta, GA) or RTP (Raleigh, NC) offices.

 

About the role

The Regulatory Science Lead (Associate Director of Regulatory Affairs) will be responsible for all regulatory activities related to product development and marketing authorizations in the US and is the primary contact point within UCB for any regulatory issues with the product and with designated health authorities.

 

Who you’ll work with

The Regulatory Science Lead (Associate Director of Regulatory Affairs) will successfully collaborate & partner with members of the US Regulatory Affairs department within the Immunology therapeutic area.  Additionally, a qualified candidate will partner with cross-functional and international teams to support UCB’s Regulatory Affairs goals.

 

What you’ll do

Develops and implements the regional regulatory strategy and plan consistent with the business objectives, inputting regional expertise into the global regulatory strategy and global planning in line with the Global Regulatory Lead.Responsible for ensuring that the regional regulatory strategy for the specific product(s), have been negotiated (if appropriate) with the regional health authorities and that the regulatory risks have been identified and mitigated.Deliver regulatory submissions in line with the applicable regulations, directives and guidelines, and in line with agreed strategies and timelines.Assist in development of regulatory standards, efficient processes and SOPs.Maintain awareness of UCB and competitors’ activities in the region and share potential impact these activities may have on the product development program.Maintain awareness of external regulatory environment, new guidelines and legislation.

 

Interested?  For this role we’re looking for the following education, experience and skills

Minimum of a Bachelor’s degree: Master’s degree preferred.A minimum of 5+ years of progressive experience in the Pharmaceutical, Biotechnology and/or CRO industry is required.10 years pharmaceutical experience in Regulatory Affairs preferred.Demonstrated experience building effective partnerships:Identifies opportunities and takes actions to build effective relationships within and across teams with appropriate use of interpersonal skills and sensitivity to diverse cultures comprising the global work environment.Proven track record of Influencing skills:Thorough well-thought through rationale and effective communication skills, able to influence key decisions.Well established communication skills:Knows when and how to communicate, using strong interpersonal skills and written communications when appropriate.Strategic and results focused:Ability to overcome obstacles and achieve key outcomesStrong Project planning and management skills:Ability to perform risk assessments, anticipating problems and providing creative solutions.

 

This positions reasonably anticipated base salary range is $141,800 - $186,100 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience, among other factors.

 

 

If you want to learn more about R&D within UCB go to R&D at UCB.

 

RANDATUCB

 

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 around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

 

Why work with us? 
At UCB, we don’t just complete tasks, we create value. We aren’t 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 equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s 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.

 

As an Equal Opportunity Employer, we are open to all talent, and adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to neurodiversity, race/ethnicity, color, national origin, religion, gender, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

 

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com 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.