Full-Time

Associate Director

Program Management, North America GM Office

Updated on 9/14/2026

BeOne

BeOne

1,001-5,000 employees

Global oncology therapeutics discovery, development, manufacturing

Compensation Overview

$148.9k - $198.9k/yr

Remote in USA

Remote

Remote within the US, with 10% travel required.

Bachelor's

Category
Project & Program Management (1)
Required Skills
Microsoft Office
JIRA
Risk Management
Marketing
Asana
Data Analysis

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Requirements
  • A bachelor's degree or BA/BS degree in business, marketing, life sciences, or a related field.
  • At least 8 years of overall experience.
  • Experience in a consulting or advisory environment, including structuring complex problems, supporting cross-functional alignment, and delivering measurable results in fast-paced, matrixed organizations.
  • Experience leading complex cross-functional and functional planning initiatives.
  • Ability to identify critical paths and risks and drive early resolution of constraints and issues with a change-management mindset.
  • Strong interpersonal and communication skills, including the ability to communicate complex ideas persuasively and concisely to broad audiences.
  • A proven track record managing digital transformation and artificial-intelligence-enabled projects from strategy through implementation.
  • Hands-on experience overseeing digital and non-personal promotion programs, including email, web, omnichannel, and programmatic channels, in a regulated pharmaceutical or life sciences environment.
  • Familiarity with artificial-intelligence tools and commercial enablement strategies, including evaluating, implementing, and driving adoption of AI-powered solutions.
  • Experience with Microsoft Office Suite and Microsoft Project or Smartsheet.
  • Familiarity with digital analytics platforms and project-management tools such as Asana, Jira, or similar tools.
Responsibilities
  • Drive the development and execution of key cross-functional commercial and medical projects across North America by establishing project plans, milestones, timelines, and accountability frameworks for on-time and on-budget delivery.
  • Build and maintain comprehensive project plans, track progress against milestones, manage interdependencies, and surface risks and issues to leadership with recommended solutions.
  • Partner with stakeholders across Medical Affairs, Market Access, Marketing, Corporate Affairs, and other functions to align projects with organizational goals and deliver within scope and budget.
  • Embed within strategic North America initiatives as a dedicated program-management resource to brand leaders and workstream leads.
  • Champion artificial-intelligence enablement across North America commercial and medical functions by identifying and implementing AI-powered tools and workflows and partnering with relevant teams to scale adoption.
  • Support digital initiatives, including digital-channel strategy, omnichannel execution, and emerging promotional technologies.
  • Monitor project schedules, milestones, and issue status; assess critical-path activities, progress, and potential risks.
  • Partner with the North America General Manager's Chief of Staff to prepare and harmonize project processes and timelines so project teams perform optimally.
  • Contribute structured analysis and sound judgment to resolve complex problems, escalate issues appropriately, and help develop practical solutions.
  • Set agendas, facilitate and document meetings, and track issues, risks, decisions, and action items.
  • Foster continuous improvement and excellence in project management.
Desired Qualifications
  • Exposure to pharmaceutical or life sciences clients in a consulting or advisory environment.

BeOne Medicines develops and commercializes cancer therapies for patients worldwide, focusing on hematologic cancers and solid tumors. Its products, including Brukinsa, are sold globally and supported by licensing partnerships, with internal R&D and clinical development driving a broad late-stage pipeline. BeOne differentiates itself by leveraging a large-scale clinical trial network and cost-efficient global drug development to achieve high margins while pursuing large-market indications. The company aims to expand into immunology and solid tumors while maintaining strong investment in R&D to make high-impact, accessible oncology treatments available in more than 45 countries.

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

Dongcheng District, China

Founded

2010

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Simplify Jobs

Simplify's Take

What believers are saying

  • August 25, 2026 FDA approval expanded TEVIMBRA in first-line HER2-positive gastroesophageal cancer.
  • August 31, 2026 Phase 3 survival data strengthened ZIIHERA-containing regimens.
  • Q2 2026 revenue hit $1.7 billion; management raised 2026 guidance to $6.8 billion.

What critics are saying

  • BeOne accepted developed-market pricing parity and Medicaid rebates on future U.S. approvals.
  • Zydus' BRUKINSA ANDA lawsuit targets patents; a 2034 composition patent remains the fortress.
  • AbbVie's trade-secrets case over BGB-16673 still threatens the BTK-degrader franchise.

What makes BeOne unique

  • BeOne built 35-plus assets and 93 trials across 1,100 U.S. sites by September 2026.
  • BRUKINSA dominates revenue, with 2026 global sales above $1.2 billion quarterly.
  • Hopewell, New Jersey gives BeOne U.S. manufacturing, R&D, and packaging capacity.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

401(k) Retirement Plan

Wellness Program

Paid Vacation

Growth & Insights and Company News

Headcount

6 month growth

6%

1 year growth

-9%

2 year growth

-3%
Yahoo Finance
Sep 4th, 2026
BeOne secures US pharma-tariff exemption after $1B+ manufacturing investment, but pricing concessions raise margin concerns

BeOne Medicines secured an exemption from Section 232 pharmaceutical tariffs through a voluntary agreement with the US government. The deal recognises over $1 billion in US manufacturing investment, including a $300 million expansion in Hopewell, New Jersey. The exemption protects BeOne from import duties on patented pharmaceuticals and ingredients. However, the company committed to pricing future FDA-approved medicines in line with other developed markets and participating in the Medicaid GENEROUS Model, which uses supplemental rebates. The Hopewell expansion will add small-molecule manufacturing and packaging capacity, creating approximately 120 full-time jobs. The facility will support a portfolio of more than 35 assets. Whilst the tariff exemption reduces supply-chain risk, international reference pricing commitments could limit pricing flexibility for future oncology medicines. Neither the tariff savings nor the financial impact of pricing concessions was disclosed.

Yahoo Finance
Aug 13th, 2026
Revolution Medicines shares rise 6.2% on BeOne-funded Phase 3 RAS(ON) deal

Revolution Medicines has partnered with BeOne Medicines in a multi-part collaboration combining BeOne's oncology assets with Revolution's four clinical RAS(ON) inhibitors. The August 2026 deal grants BeOne exclusive development and commercialisation rights in select Asian markets and commits BeOne to fund a global Phase 3 trial. Revolution Medicines reported a net loss of $644.37 million in Q2 2026 and $1.1 billion over six months. The company currently generates no revenue but projects $2.3 billion in revenue and $402.5 million in earnings by 2029. The partnership shifts near-term risk by offloading Phase 3 costs whilst providing access to milestone and royalty potential. However, the core investment case remains unchanged: regulatory progress and commercialisation of daraxonrasib, with trial execution and spending presenting the biggest risks.

Yahoo Finance
Aug 5th, 2026
BeOne Medicines Q2 revenue up 30% to $1.7B as BRUKINSA sales top $1.2B globally

BeOne Medicines reported second-quarter revenue of $1.7 billion, up 30% year over year, with GAAP earnings per ADS rising 144% to $2.05. The company's BTK inhibitor BRUKINSA generated more than $1.2 billion in global sales, increasing 31% from the prior year. The company raised its 2026 revenue guidance to CNY 6.6 billion–CNY 6.8 billion and expects GAAP operating income of CNY 1 billion–CNY 1.1 billion. Free cash flow doubled year over year to CNY 435 million. BeOne received FDA approval for Beqalzi in relapsed or refractory mantle cell lymphoma and reported positive Phase III results for a chemotherapy-free BRUKINSA regimen. US BRUKINSA sales totalled $893 million, up 31%, driven by demand in chronic lymphocytic leukaemia and non-CLL indications.

Yahoo Finance
Jul 23rd, 2026
BeOne CEO sells $34.6M in stock while retaining 50M+ shares

John Oyler, chief executive officer of BeOne Medicines AG, sold 109,713 American Depositary Shares worth $34.6 million on 20 and 21 July 2026, according to SEC filings. The transactions were executed under a Rule 10b5-1 trading plan adopted in March 2026. Despite the sale, Oyler retains a substantial ownership position exceeding 50.4 million total shares through various holdings. These include 28.2 million shares held through Oyler Investment LLC and 9.5 million shares in a Roth IRA account. The shares were sold at a weighted average price of $315.28. BeOne Medicines is a commercial-stage oncology biopharmaceutical company with $5.7 billion in trailing twelve-month revenue and a market capitalisation of $34.2 billion.

PR Newswire
Jul 21st, 2026
Seegene USA receives FDA emergency authorisation for first multiplex PCR test to diagnose viral causes of ulcerative skin lesions

Seegene USA has received Emergency Use Authorization from the FDA for its Allplex HSV-1&2/VZV/MPXV Assay, a multiplex real-time PCR test that simultaneously detects herpes simplex virus types 1 and 2, varicella-zoster virus, and monkeypox virus. It is the first multiplex PCR test designed to support differential diagnosis of viral causes of ulcerative skin lesions in the US market. These pathogens often present with similar clinical symptoms that are difficult to distinguish visually. Research presented at the 2024 Clinical Virology Symposium found that a multiplex PCR assay identified HSV, VZV, or MPXV in 54 out of 966 samples that had previously tested negative using single-pathogen methods. The assay was developed using Seegene's proprietary multiplex PCR technologies and automated product development platform.