Full-Time

Director Scientific Communications

CNS

Updated on 9/3/2026

Otsuka Pharmaceutical

Otsuka Pharmaceutical

1,001-5,000 employees

Global pharma maker of Abilify

Compensation Overview

$186.5k - $278.9k/yr

+ Incentive opportunity

Remote in USA

Remote

PharmD, PhD, MD

Category
Growth & Marketing (1)
Required Skills
Data Analysis

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Requirements
  • An advanced degree is required: Doctor of Pharmacy, Doctor of Medicine, Doctor of Philosophy, or an equivalent degree in science, medicine, or a related field.
  • At least 10 years of experience in Medical Affairs, Scientific Communications, or related roles within the pharmaceutical or biotechnology industry is required.
  • At least 3 to 5 years of prior leadership experience, including developing and managing team members, is required.
  • Demonstrated experience leading global communication strategies and integrated planning processes is required.
  • Strong experience leading cross-functional teams and influencing senior stakeholders is required.
  • The candidate must be able to translate complex scientific data into clear, strategic communication plans.
  • The candidate must have strong leadership and facilitation skills, including the ability to chair cross-functional teams.
  • The candidate must have expertise in content strategy, omnichannel engagement, and digital communication tools.
  • The candidate must have strong project management capabilities and experience managing multiple high-priority initiatives simultaneously.
  • The candidate must have executive presence and the ability to communicate effectively with stakeholders.
  • The candidate must have a strategic mindset, strong business acumen, and the ability to align scientific communications with enterprise goals.
  • The candidate must have experience leveraging innovation, including artificial intelligence and digital tools, to enhance content development and delivery.
Responsibilities
  • Lead the development and execution of a comprehensive, globally aligned medical communications strategy across assigned central nervous system assets.
  • Provide input to long-term communication priorities aligned with asset strategy, lifecycle stage, and the evolving external landscape.
  • Translate scientific and clinical insights into integrated communication approaches that support stakeholder engagement and decision-making.
  • Act as a strategic partner to senior cross-functional leaders to ensure alignment with enterprise and asset-level priorities.
  • Lead cross-functional scientific teams for assigned asset and therapeutic-area deliverables.
  • Lead the execution of Medical Communication Plans, including content strategy and deliverables, communication channels and external engagement planning, and congress execution.
  • Ensure Integrated Medical Communications Plans are integrated into annual asset planning processes and aligned with broader medical and business strategies.
  • Drive accountability for timely, high-quality execution of all Integrated Medical Communications Plan deliverables.
  • Support development and refinement of the Scientific Communication Platform, scientific narrative, and core lexicon across Medical Affairs communications.
  • Ensure consistency, clarity, and scientific rigor across all content and communication channels globally.
  • Provide strategic oversight for disease-state education materials, core field medical materials, data dissemination assets, congress-related materials, and external engagement tools.
  • Ensure content strategies are modular, scalable, and optimized for omnichannel delivery.
  • Drive the design and execution of innovative content and communication channel strategies, including digital and omnichannel engagement approaches.
  • Collaborate with internal teams to develop new tools and platforms for scientific communication, including digital, social, and interactive formats.
  • Champion emerging technologies such as artificial-intelligence-enabled content development, personalization, and automation to improve efficiency and impact.
  • Ensure content is designed for end users to enhance accessibility, engagement, and scientific understanding.
  • Serve as a core leader within cross-functional asset teams.
  • Translate emerging clinical data into actionable communication strategies.
  • Ensure alignment and appropriate scientific integration across global and regional initiatives while maintaining Medical Affairs independence.
  • Ensure communications are scientifically accurate, evidence-based, and compliant with internal policies and external regulations.
  • Establish and oversee governance frameworks for content development, review, and lifecycle management.
  • Act as an escalation point for complex scientific or compliance-related content decisions.
  • Maintain high standards of quality, consistency, and ethical communication practices.
  • Lead annual scope-of-work planning and resource allocation for scientific communications deliverables.
  • Oversee agency partnerships, including selection, contracting, performance management, and optimization.
  • Drive operational excellence, process improvements, and scalable content development models.
  • Ensure efficient delivery of high-quality outputs within budget and timelines.
  • Lead, develop, and mentor a high-performing team of Associate Directors, Managers, and cross-functional contributors.
  • Foster a culture of scientific excellence, innovation, accountability, and collaboration.
  • Build organizational capability in scientific communications, including best-practice sharing and process standardization.
  • Promote a learner-first, inclusive mindset in content development and team culture.
  • Stay current with advancements in scientific communications, digital engagement, and the external healthcare landscape.
  • Gather and implement best practices across regions to drive consistency and innovation.
  • Use insights, analytics, and stakeholder feedback to continuously optimize communication strategies and execution.
Desired Qualifications
  • Experience in the central nervous system therapeutic area.
Otsuka Pharmaceutical

Otsuka Pharmaceutical

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Otsuka Pharmaceutical develops and markets medicines and health products worldwide, including prescription drugs and nutraceutical beverages. Its product lineup ranges from pharmaceutical treatments such as Abilify (an antipsychotic) to consumer health drinks like Pocari Sweat, which helps replenish electrolytes. Abilify works as a psychiatric medication used to treat conditions such as schizophrenia and bipolar disorder, while Pocari Sweat is an ion-replacement beverage designed to restore minerals and fluids after activity or heat. The company differentiates itself through a long history dating back to its founding in 1921, a broad, globally scaled portfolio spanning drugs and health beverages, and a focus on health improvements across populations. Its stated goal is to create new products for better health worldwide.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

Tokyo, Japan

Founded

1921

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Simplify Jobs

Simplify's Take

What believers are saying

  • Otsuka closed Transcend in June 2026, expanding psychiatry beyond Abilify dependence.
  • DAWNZERA gained EU authorization in January 2026, opening paid sales across 27 countries.
  • Paradise uRDN and CART BP pro broaden Japan's hypertension platform and device distribution.

What critics are saying

  • SIMTRIYO waits on DEA scheduling, delaying revenue until late 2026.
  • VOYXACT's accelerated approval depends on confirmatory kidney-outcome data; failure risks withdrawal.
  • Transcend's TSND-201 PTSD program remains clinical-stage, risking a $1.225 billion write-down.

What makes Otsuka Pharmaceutical unique

  • Otsuka pairs CNS, nephrology, and device assets across Japan, US, and Europe.
  • SIMTRIYO gives Otsuka a first-in-class ADHD stimulant franchise after July 2026 FDA approval.
  • DAWNZERA and VOYXACT anchor rare-disease pipelines with global reimbursement and accelerated paths.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Company Match

Tuition Reimbursement

Student Loan Assistance

Paid Holidays

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
Associated Press
Jul 25th, 2026
FDA approves Otsuka's Simtriyo, first-in-class ADHD treatment for adults and children 6+

Otsuka Pharmaceutical has received FDA approval for SIMTRIYO (centanafadine), the first norepinephrine, dopamine, serotonin reuptake inhibitor for treating ADHD in adults and children aged six years and older weighing at least 20kg. The once-daily extended-release capsule will be available later this year following DEA scheduling. The approval is based on four Phase 3 clinical trials showing statistically significant improvements in ADHD symptoms compared to placebo, with benefits observed as early as week one. Common side effects include decreased appetite, nausea, rash, and headache. ADHD affects approximately 7 million children and 15.5 million adults in the US. The drug carries boxed warnings for suicidal ideation in pediatric patients and potential for abuse and addiction.

SonoThera
Jun 10th, 2026
SonoThera Closes Oversubscribed $125 Million Series B Financing to Advance Clinical Development of Ultrasound-Mediated Nonviral Genetic Medicines - SonoThera

SAN FRANCISCO–SonoThera, a biotechnology company developing next-generation genetic medicines to address the root causes of disease, today announced the closing of an oversubscribed $125 million Series B financing round to advance its lead programs in Duchenne muscular dystrophy (DMD) and autosomal dominant polycystic kidney disease (ADPKD) into the clinic and expand its pipeline of targeted, redosable genetic medicines.

Dealroom.co
Mar 27th, 2026
Transcend Therapeutics company information, funding & investors

Transcend Therapeutics, developing the next generation of psychoactive compounds for neuropsychiatry focused on patient access. Here you'll find information about their funding, investors and team.

Fierce Biotech
Mar 27th, 2026
Otsuka buys Transcend Therapeutics for $700M upfront in psychiatric drugs deal

Otsuka Pharmaceutical has acquired Transcend Therapeutics for $700 million upfront through its subsidiary Otsuka America, with potential milestone payments of up to $525 million. The deal gives Otsuka access to Transcend's MDMA analogue for psychiatric conditions currently in development.

Associated Press
Mar 25th, 2026
Otsuka's Voyxact shows 82.5% hematuria improvement in IgA nephropathy trial at 48 weeks

Otsuka presented new Phase 3 VISIONARY trial data for VOYXACT (sibeprenlimab-szsi) in IgA nephropathy patients at the 2026 ISN World Congress of Nephrology. The analyses showed 82.5% of patients receiving sibeprenlimab achieved negative microscopic hematuria at week 48, compared with 52.6% on placebo. Median time to achieve hematuria negativity was nine weeks versus 24 weeks for placebo. VOYXACT, approved under accelerated approval in the US, is a monoclonal antibody that inhibits APRIL, a key driver in IgAN pathogenesis. Previously reported data showed the drug met its primary endpoint with a 51.2% placebo-adjusted reduction in proteinuria at nine months. The trial continues evaluating sibeprenlimab's effect on preserving kidney function over 24 months.