Global Clinical Development Director (CNS & Digital) Remote

Otsuka America Pharmaceutical Inc.

Lincoln (NE)

Remote

USD 230.000 - 360.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Otsuka America Pharmaceutical Inc. is seeking a Senior Director, Global Clinical Development to lead design and oversight of clinical programs for OPDC products, focusing on CNS and Digital Medicine. Remote or office-based in the U.S., with collaboration across global teams and regulators.

The role requires MD/DO with extensive clinical and regulatory experience, strong leadership, and the ability to travel up to 30% to support trials and regulatory activities.

Qualifikationen

  • Clinician (MD or DO) with management experience.
  • Experience in pharmaceutical industry or academic translational clinical research.
  • Strong communication skills in meetings and written forms.
  • Knowledge of global regulatory filings.
  • Understanding of drug development and clinical trial management.
  • Willingness to travel 30% internationally.

Aufgaben

  • Designs and oversees clinical research programs and protocols for OPDC-GCD.
  • Evaluates and develops CNS and Digital Medicine products across development stages.
  • Communicates with patients, clinicians, regulators, and teams to optimize trial objectives and plans.
  • Authors program strategies and oversees trials for safety, efficacy, and value.
  • Provides strategic oversight of vendor/CRO relationships and governance.

Kenntnisse

Clinical medicine
Team leadership
Communication
Regulatory knowledge

Ausbildung

MD/DO required

Tools

Microsoft Office

Jobbeschreibung

Otsuka America Pharmaceutical Inc. is seeking a Senior Director, Global Clinical Development to lead design and oversight of clinical programs for OPDC products, focusing on CNS and Digital Medicine. Remote or office-based in the U.S., with collaboration across global teams and regulators.

The role requires MD/DO with extensive clinical and regulatory experience, strong leadership, and the ability to travel up to 30% to support trials and regulatory activities.

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