Job Description

We are looking for a talented individual to fill the position of: Content Lifecycle Partner

As the Content Lifecycle Partner, you will serve as the business partner for the material review processes (also known as Review Committee or Medical-Legal-Regulatory Review) by facilitating processes to deliver optimal outcomes aligned to strategic priorities. You will serve as a daily leader for the review and approval of high impact content and materials initiatives, focusing on stakeholder collaboration and process efficiencies. You will provide initial feedback on alignment of content to UCB guidelines and ensure feedback is provided from designated stakeholder. You will be asked to contribute to special projects that enhance content creation and review processes as well as contribute to training curriculum implementation and delivery.

You like to work in an environment where you can: 

• Coordinate and facilitate effective and efficient MRL review meetings, managing the needs of cross-functional stakeholders. Understand OPDP promotional labeling regulations and guidelines for the successful and compliant commercial marketing of UCB products.
• Forecast demand for MRL review and approval of materials for assigned brands. Establish and maintain strategic trusting relationships with cross-functional stakeholders, guiding and influencing collaborative activities and mutual decision-making.
• Contribute and participate in developing company processes, practices, and policies relevant to the creation, review and approval of promotional and scientific exchange materials.
• Develop and oversee agency vendor standards, co-create performance measures and provide periodic feedback to business partners to ensure optimal alignment and performance.

You will contribute by: 

• Managing deliverables to align with changing business environments by fostering collaborative, efficient, and effective working relations with internal and external stakeholders related to content life cycle management (planning, review and approvals, end stage lifecycle).
• Collaborating to achieve objectives of stakeholders of the material review process by contributing information and recommendations to material development timelines. In collaboration with UCB Governance Partners, ensure the management and maintenance of records and databases that support communication with OPDP and internal documentation standards.
• Working to resolve problems, identify trends, determining system improvements and recommends/implements change to increase efficiency of the review process
• Being responsible for the performance of the CLM processes, measuring/capturing and using clearly defined KPI’s

Interested? For this position you’ll need the following education, experience and skills: 

• Minimum Qualifications:
• Bachelors Degree
• 3 years of project management experience in the pharmaceutical, biotech, medical device industry or 3 years of experience working within an agency servicing the pharmaceutical industry

Preferred Qualifications:

• Masters Degree
• Advanced knowledge of US regulations for the promotion of pharmaceutical and biological products
• Proficiency in PPT, Excel, Word, MS Teams, Veeva
• Process Management and Improvement
• Stakeholder Management
• Complex decision making
• Why you should apply

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve. If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.

About Us

At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.

With a team of approximately 7,500 employees worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.

Curious to know more? Please visit our website www.ucb.com.

How to Apply

Job Categories: Equal Opportunities. Job Types: Full-Time. Salaries: Not Disclosed.

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