Job Title: Senior Manager Global Medical Affairs Resources
Job Location: Great Britain United Kingdom
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
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 with be responsible for creating and maintaining Medical Affairs slide decks and will collaborate with Medical Affairs stakeholders to create highquality evidencebased medical content for use in internal training external scientific exchange and digital platforms. This is a remotebased role with no direct reports
Essential Functions Of The Job
Under the leadership of the Associate Director Global Resource Lead collaborate crossfunctionally 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 ontime delivery of resources; effectively communicate project timelines and project status to stakeholders.
Anticipate and mitigate risks to ontime 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 countryspecific 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 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
SelfAwareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
ResultsOriented
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.
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