Content Clearance Lead

Make your mark for patients

We are looking for a Content Clearance Lead who is intellectually curious, self-driven, and adaptable to join our the Omnichannel and Content Operations team based in our Atlanta, Georgia office in the United States. This hybrid position requires a minimum of 40% on site presence and up to 10% domestic/international travel.

About the role
You will serve as the US business partner for the content clearance process (Review Committee or Medical-Legal-Regulatory Review) consisting of promotional and non-promotional materials. The Lead manages the review, discussion and approval of content, materials, and initiatives, with application and interpretation of regulations and industry guidance.

Who you'll work with
You will work with Regulatory, Legal, Compliance, Medical Leads, Marketing Leads, Market Access, Patient Value Units, as well as all cross functional Subject Matter Experts and stakeholders that have input into the strategy and creation of promotional and non-promotional material.

What you'll do

• Perform initial quality reviews of materials and route submissions per internal governance standards.
• Act as a Chair for Clearance Committees and lead efficient, effective content review meetings.
• Partner with stakeholders to define project timelines, manage priorities, and advise on content processes.
• Forecast review demand and manage approvals across planning, review, health authority submissions, dissemination and withdrawal lifecycle stages.
• Ensure compliance with UCB standards and U.S. promotional labeling regulations.
• Drive continuous improvement through retrospectives, deviation tracking, and root cause analysis.
  
  

Interested? For this role we're looking for the following education, experience and skills
Minimum Education, Qualifications, Skills

• Bachelor's degree
• 5+ years of experience in pharmaceutical industry or life sciences industry, preferably in controlled process environment including development and approval of regulated information and materials.
• Intermediate to advanced knowledge of US regulations for the promotion of pharmaceutical and biological products with proficiency in identifying emerging issues and making recommendations for resolution.
• Ability to support multiple products or indications in all lifecycle stages; interpret and apply strategic business objectives to the clearance and ad/promo domain.
• Excellent organization, time management, planning, and prioritization skills, with attention to detail.
• Proven ability to work collaboratively and with sensitivity in a matrix organization.
• Demonstrated aptitude for producing clear, concise verbal and written communications
  

The reasonably anticipated salary range for this position is $108,000-$141,800 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 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 equal 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.

At UCB, we've 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 employer. All 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 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.