Full-Time

Associate Director

Medical Publications, CNS

Otsuka Pharmaceutical

Otsuka Pharmaceutical

1,001-5,000 employees

Global pharma maker of Abilify

Compensation Overview

$169.2k - $253k/yr

+ Incentive opportunity

Remote in USA

Remote

PharmD, PhD, MD

Category
Biology & Biotech (1)
Required Skills
Forecasting
Financial analysis

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Requirements
  • An advanced scientific or medical degree, such as a PharmD, PhD, MD, or equivalent, is required.
  • At least 7 years of experience in Medical Affairs, Scientific Communications, or related roles within the pharmaceutical or biotechnology industry or a related field is required.
  • Experience supporting publication planning and execution for global or regional programs is required.
  • Experience working with external vendors and medical writers is required.
  • Strong project management and organizational skills are required to manage multiple concurrent deliverables.
  • Excellent written and verbal communication skills and strong attention to scientific accuracy are required.
  • A solid understanding of Good Publication Practices, ICMJE guidelines, and industry standards is required.
  • Strong cross-functional collaboration and stakeholder management skills are required.
  • The ability to contribute to strategic discussions while maintaining a strong execution focus is required.
  • Experience supporting vendor management and operational workflows is required.
  • Financial awareness and experience supporting budget tracking and management are required.
Responsibilities
  • Support implementation and execution of publication plans for CNS assets, ensuring alignment with medical strategy, data dissemination priorities, and product lifecycle needs.
  • Collaborate with cross-functional teams to define publication timelines, data prioritization, and congress and journal strategies.
  • Lead the end-to-end development of publication deliverables, including abstracts, posters, and manuscripts.
  • Ensure scientific accuracy, quality, and compliance with Good Publication Practices, ICMJE, and company standard operating procedures.
  • Contribute to integrating publications within broader scientific communication platforms, ensuring consistency across materials.
  • Identify opportunities to improve workflows and operational efficiency, including the use of technology and artificial intelligence-enabled tools.
  • Manage day-to-day interactions with publication vendors and medical writing partners to ensure timely, high-quality deliverables.
  • Provide direction, feedback, and review of vendor outputs to ensure alignment with scientific and compliance standards.
  • Support budget tracking, forecasting, and reconciliation for publication-related activities.
  • Partner with Clinical Development, Global Integrated Evidence & Innovation, Medical Strategy, and Medical Communications teams to support data readiness and timely dissemination of clinical results.
  • Serve as a key point of contact for publication execution within the CNS Medical Communications team.
  • Collaborate with Field Medical and Medical Communications teams to ensure alignment and consistency of messaging across medical materials.
  • Support integrated medical communications planning and contribute to launch and lifecycle initiatives.
  • Ensure all publication activities adhere to internal standard operating procedures, Good Publication Practices, ICMJE, and applicable regulatory requirements.
  • Collaborate with Legal, Regulatory, and Compliance functions to ensure appropriate governance and ethical publication practices.
  • Maintain accurate documentation and support audit readiness.
Desired Qualifications
  • Experience in the CNS or a related therapeutic area is preferred.
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.