Remote Clinical Development Director – CNS Digital Medicine

Otsuka America Pharmaceutical Inc.

Bismarck (ND)

Remote

USD 250,000 - 388,000

Full time

10 days ago

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Benefits offered by this job

Comprehensive medical
Dental
Vision
401(k) match
Tuition reimbursement

Job summary

Otsuka America Pharmaceutical Inc. is seeking a Senior Director, Global Clinical Development, remote-based or in Rockville, MD or Princeton, NJ, to lead design and oversight of clinical research programs for OPDC products.

The role spans CNS and digital medicine across development stages, with responsibility for strategies, trial design, and regulatory filings. The position requires medical/clinical expertise, management experience, and strong communication; travel 30% domestically and

Qualifications

  • Medical doctor with clinical leadership background and pharma/clinical research exposure.
  • Experience in pharmaceutical industry or translational clinical research.
  • Ability to define objectives and manage projects to timelines and budget.
  • Strong written and oral communication skills; regulatory filings experience is a plus.
  • Willingness to travel ~30% (domestic and international).

Responsibilities

  • Design and oversee clinical research programs and protocols for OPDC products.
  • Evaluate and develop CNS and digital medicine programs across development stages.
  • Lead regulatory filings and clinical study documentation.
  • Provide strategic direction for vendor/CRO relationships and governance.
  • Support life-cycle management and value-driven development strategies.

Skills

Clinical leadership
Management experience
Clinical development
Regulatory understanding
Travel readiness

Education

MD/DO
PhD/MPH/MBA a plus

Tools

Microsoft Office

Job description

Otsuka America Pharmaceutical Inc. is seeking a Senior Director, Global Clinical Development, remote-based or in Rockville, MD or Princeton, NJ, to lead design and oversight of clinical research programs for OPDC products.

The role spans CNS and digital medicine across development stages, with responsibility for strategies, trial design, and regulatory filings. The position requires medical/clinical expertise, management experience, and strong communication; travel 30% domestically and

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