Senior Manager, Global Medical Affairs Resources

BeiGene, Inc.; United Kingdom; Remote; GBP 45,000 - 80,000

Job description

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The candidate will be responsible for creating and maintaining Medical Affairs slide decks and will collaborate with Medical Affairs stakeholders to create high-quality, evidence-based medical content for use in internal training, external scientific exchange, and digital platforms. This is a remote-based role with no direct reports.

Essential Functions of the job:

Under the leadership of the Associate Director, Global Resource Lead, collaborate cross-functionally to develop scientific resources, including scientific/clinical slide decks, field resources, and digital content for external use by Global Medical Affairs.

• Liaise with Global Publication Planning Leads and monitor the medical literature and conference abstracts for new reports in the therapeutic area for inclusion in Medical Affairs resources.
• Incorporate insights into medical resource development and ensure alignment with Medical strategy.
• Conduct literature searches and analyze results to identify scientifically robust supporting references for Medical Affairs resources.
• Coordinate resource development with internal subject matter experts.
• Work with Medical Affairs colleagues to develop project timelines and ensure on-time delivery of resources; effectively communicate project timelines and project status to stakeholders.
• Anticipate and mitigate risks to on-time delivery.
• Develop and maintain slide deck templates, including layouts, formats, colors, and style guides, working with or managing vendors as needed.
• Evaluate and interpret medical insights, medical strategy, and stakeholder expertise to identify, develop, and update materials appropriately.
• Medical/scientific content development to support omnichannel and digital initiatives.
• Collaborate with Global Medical Affairs stakeholders to ensure global resources meet regional needs and develop local or country-specific resources as needed. Ensure that key data statements and conclusions are consistent across related assets.
• Manage all technical aspects of Medical Review Committee (MRC) reviews and approvals for new or updated Medical Affairs slide decks, including annotations, referencing, and comment adjudication, in collaboration with clinical subject matter experts and MRC members and administrators.
• Contribute to annual content planning cycles and support the development of global training projects and initiatives.
• Adhere to BeiGene SOPs, work instructions, and quality standards.
• Apply legal, regulatory, and compliance requirements to all Medical Affairs activities.

Education Required:

• MS degree or higher (PhD or Pharm.D) required.

Qualifications:

• MA/MS degree with 5+ years or a PhD/PharmD with 3+ years of experience in pharmaceutical or agency medical affairs required.
• 3+ years of experience creating scientific resources in a pharmaceutical, biotech, or agency/vendor setting for delivery to healthcare professionals and payors.
• Scientific/clinical background in hematology and/or oncology, preferred.
• Digital omnichannel delivery of scientific content experience preferred.
• Excellent interpersonal communication, presentation, strong personal integrity, teamwork abilities, and customer focus are necessary with demonstrated superior written and verbal communication skills required.
• Knowledge of science and healthcare, including the ability to learn new concepts and new therapeutic areas quickly.
• Demonstrated ability in project management, prioritization, and strong organizational skills.
• Knowledge of clinical medicine, disease management, and medical research practices preferred.
• Demonstrated ability to manage projects and to effectively coach, mentor, and communicate with scientific/clinical persons at all skill and knowledge levels.
• Knowledge of applicable international compliance guidelines and regulations for scientific communications applicable to pharmaceutical companies.
• Experience in vendor management.
• Confident, positive attitude, enthusiastic and charismatic.

Supervisory Responsibilities:

• None

Computer Skills:

• Expert working knowledge of Microsoft Office Suite.
• Expertise in Adobe Creative Suite including Illustrator preferred.
• Experience in Veeva strongly preferred.
• Familiarity with SharePoint and project management software preferred.

Location:

• Remote

Travel: Work-related travel approximately 15-25%.

BeiGene Global Competencies

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity, and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

• Fosters Teamwork
• Provides and Solicits Honest and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial Mindset
• Continuous Learning
• Embraces Change
• Results-Oriented
• Analytical Thinking/Data Analysis
• Financial Excellence
• Communicates with Clarity

We are proud to be an equal opportunity employer and we value diversity. BeiGene does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.