Senior Project Lead Programmer, Raleigh, NC
Raleigh, WV - USA
Job Summary
Make your mark for patients
We are looking for a Senior Project Lead Programmer who is strategic collaborative and innovative to join us in our Biometrics and Data Science team based in our Raleigh NC office in the United States.
About the role
In this role you will serve as the senior programming leader for one or more complex clinical development programs. You will lead programming strategy delivery and innovation across the full drug development lifecycle partnering closely with global crossfunctional teams. You will shape modern programming practices ensure highquality regulatory submissions and play a visible role in advancing datadriven decision making across the organization.
Who youll work with
You will work within the Biometrics and Data Science organization collaborating with statisticians data scientists clinical leaders regulatory partners and external vendors. You will act as the primary programming representative on compound or project teams working across geographies and functions to deliver highimpact results in a fastmoving global environment.
What youll do
- Lead programming strategy and delivery for complex clinical development programs
- Serve as primary programming representative on crossfunctional project teams
- Drive innovation in statistical programming methods tools and operating models
- Ensure highquality compliant programming deliverables for regulatory submissions
- Lead coach and develop global programming teams and external partners
- Represent the organization in crossindustry initiatives and scientific forums
Interested For this role were looking for the following
Minimum requirements
- Masters degree in statistics computer science life sciences or related discipline
- Minimum of 10 years of experience in statistical programming within the pharmaceutical industry
- Minimum of 5 years of experience leading complex programs or global programming teams
- Minimum of 6 years of experience in people leadership including managers or senior leads
Preferred requirements
- Advanced programming expertise using SAS R or similar languages
- Strong knowledge of clinical trial standards and regulatory submission requirements
- Experience leading global regulatory submissions and health authority interactions
- Proven track record in driving innovation and operating model transformation
- Active participation in external data analytics or programming communities
This positions reasonably anticipated salary range is $184k-$241k per year. The actual salary offered will take into account internal equity and also may vary depending on the candidates geographic region job-related knowledge skills and experience among other factors.
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.
Required Experience:
Senior IC
About Company
UCB – Inspired by patients. Driven by science. At UCB, we put our heart, soul and skills into making a difference for people living with severe diseases. We're here because we want to transform patients’ lives by pushing the boundaries of what is possible.To achieve our ambition, we w ... View more