Senior Medical Science Liaison - Remote & KOL Engagement

Takeda

Lorida (FL)

Remote

USD 120,000 - 170,000

Full time

10 days ago

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Job summary

Takeda US Medical seeks an experienced Medical Science Liaison (MSL) to build and maintain relationships with KOLs and HCPs across territories, aligning with medical strategy. You will analyze complex data, disseminate it responsibly, and support sponsored and investigator-initiated studies.

You will collaborate with cross-functional teams, travel up to 70%, and ensure timely, compliant documentation of activities and insights within a virtual environment.

Qualifications

  • Minimum of 2 years of field-based MSL experience in pharma required.
  • Dissemination of complex scientific data to healthcare audiences.
  • Clinical, research, and/or teaching experience.
  • Ability to work effectively in virtual and cross-functional teams.
  • Execution of activities within regulatory and compliance requirements.

Responsibilities

  • Build and maintain professional relationships with KOLs/HCPs per territory plans.
  • Analyze and interpret complex scientific information for dissemination to KOLs/HCPs in a fair-balanced manner.
  • Support Takeda-sponsored research and assist with investigator-initiated studies.
  • Communicate medical insights to refine strategies and tactics.
  • Identify partnerships between KOLs/HCPs and Takeda US Medical.
  • Participate in medical strategy at conferences and staff booths.
  • Respond to unsolicited HCP medical information inquiries per Medical Information.
  • Complete CRM entries, insights capture, training, expense reporting and admin tasks in a compliant manner.

Skills

MSL experience
KOL engagement
Medical strategy
Cross-functional teams

Education

PharmD/MD/PhD
MSN/NP/PA minimum

Job description

Takeda US Medical seeks an experienced Medical Science Liaison (MSL) to build and maintain relationships with KOLs and HCPs across territories, aligning with medical strategy. You will analyze complex data, disseminate it responsibly, and support sponsored and investigator-initiated studies.

You will collaborate with cross-functional teams, travel up to 70%, and ensure timely, compliant documentation of activities and insights within a virtual environment.

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