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Job Description

Primary Duties

  • Serve as a field-based extension of the Therapeutic Area Medical Strategy Group
  • Systematically identify the scientific exchange needs of Key Opinion Leaders (KOLs), investigators and other stakeholders in patient care, establish strong professional relationships, provide credible scientific expertise and serve as a liaison to Takeda Global Medical, Global Clinical and external partners
  • Ensure compliant communication and education of Takeda’s marketed and emerging product portfolio to
  • meet the educational and professional needs of Takeda’s key customers
  • Responds effectively to requests for scientific exchange
  • Support local team disease area and product knowledge through scientific training
  • Maintain personal expertise in relevant disease areas and MSL best practices

Responsibilities

KOL Relationship Management:

  • Through compliant scientific exchange, builds and maintains professional relationships with external stakeholders to expand Takeda’s research, advisory and educational partnership
  • opportunities
  • Ensures high standard of professionalism to develop and maintain “peer-to-peer” scientific relationships with key thought leaders in healthcare, academia, payer, and government
  • organizations per strategic territory plans and as requested by KOLs, including the management of strategic scientific partnerships and scientific exchange
  • Provide scientific liaison support to Investigators currently involved in the Takeda’s Company sponsored interventional or observational studies and investigator-initiated trials
  • Engage KOLs through various planned scientific activities, to increase awareness on disease perception for TA as per Takeda norms and SOPs
  • Facilitate 1:1 and group scientific interactions with healthcare professionals
  • Maintain KOL profile, plans and insights including updating medical customer relationship management system in a timely, accurate, and compliant manner
  • Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchange, and coordinate high-quality interactions between these resources and external customers

Effective and Compliant Dissemination of Data including HCP education and disease awareness

  • Presents clinical and disease state information to a variety of audiences, including KOLs,
  • Medical advisors, formulary/decision makers and other HCPs and Takeda internal teams
  • Respond within defined timeline and quality standards to unsolicited inquiries from HCPs and other stakeholders received by Global Medical Affairs
  • Drive, support and execute presentation of scientific evidence and medical education amongst physician community in assigned TA
  • Ensures appropriate scientific exchange with HCPs by fostering fair and balanced medical and scientific communications that are not misleading
  • Serves as scientific resource at key medical, scientific, and patient advocacy conferences as assigned
  • Conducts therapeutic training for Sales and Medical colleagues upon request

Contribute to Takeda’s Strategic Medical Strategy

  • Provide scientific input and participate in local medical and cross-functional initiatives
  • Provide field-based medical support to Takeda’s clinical research programs, registries, and facilitation of the investigator sponsored trials process
  • Communicates key medical insights from KOLs/HCPs to inform refinement of medical strategies or tactics
  • Gains customer insights, opinions and feedback and engages with internal colleagues to connect business opportunities with internal resources
  • Under the guidance of TA Lead for GI and Immnology, provides scientific support for company-sponsored meetings
  • Participates on internal project teams as directed by Management (e.g. publications)

Maintaining personal expertise in relevant disease areas and MSL best practices

  • Maintain knowledge base and scientific expertise on all assigned Takeda disease areas and products
  • Develop and update knowledge of applicable pharmaceutical guidelines and regulations, including, but not limited to, ICH, GCP, PhRMA, DOJ, OIG, R&D Code of Ethical Practices and company policies
  • Develop/increase knowledge of medical literature and critical appraisal of scientific publications

Locations

IND - Remote Location

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

#LI-Remote

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Deadline: 25-06-2024

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