Associate Medical Director, Clinical Science - Lead Global Trials

Takeda Pharmaceutical Co.

Cambridge (MA)

Hybrid

USD 199.000 - 312.000

Vollzeit

Vor 9 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Takeda Pharmaceutical Co. in Cambridge, MA is seeking an Associate Medical Director, Clinical Science for the GI2 TAU to lead clinical science activities, influence development plans, and drive strategy within a hybrid work model.

The role involves leading protocol development, trial monitoring, interactions with key opinion leaders, and cross-functional collaboration to ensure regulatory readiness and scientific integrity.

Qualifikationen

  • MD or international degree with 3+ years clinical research in pharma/biotech or academia
  • Immunology subspecialty preferred
  • Phase 3 clinical trial experience preferred
  • Experience leading matrix teams preferred
  • Management experience preferred
  • Strong communication and negotiation skills emphasized

Aufgaben

  • Represent Clinical Science on project teams and lead as Clinical Science leader
  • Guide Clinical Development Plan and CDP documents for study execution
  • Monitor safety and data; adjust development plans as needed
  • Interact with key opinion leaders and regulatory bodies
  • Oversee trial monitoring and protocol development
  • Lead cross-functional collaboration to align strategy

Kenntnisse

MD or international degree
Phase 3 trials experience
Immunology subspecialty
Managing matrix teams
Leadership experience
Strong communication
Negotiation skills
GCP/ICH knowledge
Travel willingness

Ausbildung

MD or internationally recognized equivalent

Jobbeschreibung

Takeda Pharmaceutical Co. in Cambridge, MA is seeking an Associate Medical Director, Clinical Science for the GI2 TAU to lead clinical science activities, influence development plans, and drive strategy within a hybrid work model.

The role involves leading protocol development, trial monitoring, interactions with key opinion leaders, and cross-functional collaboration to ensure regulatory readiness and scientific integrity.

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