Z

Zymeworks

Biopharmaceutical firm developing multifunctional therapeutics

Senior Program Manager - Clinical

Full-TimeUpdated on 10/25/2026
CA$105k - CA$195.5k/yr+ Employee Share Purchase Program + Employee Equity Program
Senior
Bachelor's
Bellevue, WA, USA+1 moreMore locations: Vancouver, BC, Canada
HybridHybrid, with a minimum of 3 days per week onsite.
Biology & BiotechClinical Research Operations
No H1B Sponsorship

About the job

Requirements
  • A Bachelor of Science degree in a biological science.
  • At least six years of project-management experience in the bioscience industry.
  • Experience with multiple external partnerships and the ability to manage multiple simultaneous projects.
  • Broad knowledge of early-stage development of new biologics.
  • The ability to achieve results through other managers and people.
  • Strong written and oral communication and presentation skills.
Responsibilities
  • Support project management for early-stage clinical programs and work with the Project Leader to track tasks while considering timelines and budget.
  • Develop and implement a new matrixed Product Development Team framework with input from cross-functional partners, including Clinical, Preclinical, CMC, and Commercial.
  • Manage the project planning process, track project timelines, and drive execution.
  • In collaboration with the Team Lead, manage Product Development Team meetings across different programs.
  • Work across functional areas to ensure Clinical Development maintains project timelines and budgets, collaborating with preclinical, CMC, finance, and other groups within Zymeworks.
  • Identify issues, analyze risks, and develop contingency plans to support the Clinical Project Leader and Clinical Development team.
  • Partner with the Zymeworks Clinical team to ensure study timelines and budgets are achieved.
  • Communicate and coordinate with internal and external stakeholders as needed.
  • Prepare and manage overall clinical and product development plans for each clinical program, including associated timelines and budget information.
  • Liaise with preclinical project teams and Clinical Development teams to identify gaps and accelerate preclinical programs toward Phase I/II clinical trials.
  • Oversee program budgets and maintain forecasts for annual operating expenditures and departmental expenses.
Desired Qualifications
  • PMP certification.

About the company

Zymeworks develops multifunctional therapeutics for hard-to-treat cancers and other serious diseases. Its main products are antibody-drug conjugates (ADCs) and multispecific (bispecific) antibodies that link cancer targets to therapeutic payloads using proprietary platforms for precise engagement and modular design. The company drives discovery, preclinical work, and clinical development with an integrated R&D engine and earns revenue through partnerships, licensing, and commercialization of its own therapies. Its goal is to discover, develop, and commercialize novel therapeutic agents globally to improve outcomes for patients with difficult-to-treat cancers and other serious diseases.

Company Size

201-500

Company Stage

IPO

Headquarters

Vancouver, Canada

Founded

2003

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Simplify's Take

What believers are saying

  • FDA approved Ziihera for first-line HER2+ GEA on August 25, 2026.
  • Completed Theravance on September 23, 2026, raising 2026 revenue guidance to $278 million-$292 million.
  • Hospital YUPELRI sales grew 25% year over year in Q2 2026.

What critics are saying

  • Zymeworks depends on Ziihera, YUPELRI, and partner sales; any stumble hits 2027 cash flow.
  • The $350 million OMERS note sweeps 75% of YUPELRI cash until repayment.
  • Leadership churn in January 2026 and ZW191 readouts can derail execution by Q1 2027.

What makes Zymeworks unique

  • Ziihera’s HER2 bispecific plus Azymetric platform creates differentiated oncology economics.
  • September 2026 Theravance added YUPELRI cash flow, royalties, and commercial infrastructure.
  • ZW191 uses proprietary FRα ADC chemistry and a novel ZD06519 payload.

Help us improve and share your feedback! Did you find this helpful?

Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Wellness Program
  • 401(k) Company Match
  • Company Equity
  • Paid Vacation
  • Hybrid Work Options
  • Remote Work Options
  • Employee Share Purchase Program

Growth & Insights and Company News

6 month growth

0%

1 year growth

1%

2 year growth

3%
Yahoo Finance
Oct 19th, 2026
Zymeworks appoints Suzanne Monahan to lead Theravance Biopharma and YUPELRI commercial strategy

Zymeworks has appointed Suzanne Monahan as senior vice president, commercial, and general manager of Theravance Biopharma, effective immediately. She will report to Kenneth Galbraith, chair and chief executive officer. Monahan will lead commercial strategy for YUPELRI (revefenacin), the first and only once-daily nebulised long-acting muscarinic antagonist approved in the US for maintaining treatment of chronic obstructive pulmonary disease. Zymeworks recently acquired Theravance Biopharma. Monahan has more than 20 years of commercial experience in pharmaceuticals and medical devices. She most recently served as senior vice president at Pacira BioSciences, and earlier worked at Shionogi, Circassia Pharmaceuticals, Sanofi-Aventis, and Salix Pharmaceuticals. "Suzanne is a proven commercial leader," Galbraith said.

The Pharma Letter
Oct 19th, 2026
Zymeworks hires Pacira commercial exec Suzanne Monahan to run Yupelri business after Theravance deal.

Zymeworks hires Pacira commercial exec Suzanne Monahan to run Yupelri business after Theravance deal. 19 October 2026 Vancouver-based biotech Zymeworks (Nasdaq: ZYME) has appointed Suzanne Monahan as senior vice president, commercial, and general manager of Theravance Biopharma, effective immediately. She reports to Kenneth Galbraith, Zymeworks' chair and chief executive. This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here. Try before you buy Free. 7 day trial access * All the news that moves the needle in pharma and biotech * Exclusive features, podcasts, interviews, data analyses and commentary from its global network of life sciences reporters. * Receive The Pharma Letter daily news bulletin, free forever. Become a subscriber £820. Or £77 per month * Unfettered access to industry-leading news, commentary and analysis in pharma and biotech. * Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results. * Daily roundup of key events in pharma and biotech. * Monthly in-depth briefings on Boardroom appointments and M&A news. * Choose from a cost-effective annual package or a flexible monthly subscription The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It's part of the key information for keeping me informed Chairman, Sanofi Aventis UK More on this story... 29 June 2026 3 June 2026 14 October 2026 Companies featured in this story. Sign up to receive email updates Join industry leaders for a daily roundup of biotech & pharma news Today's issue. 19 October 2026 Company spotlight. A clinical-stage AI-driven drug discovery company whose HER2 inhibitor IAM1363 is showing brain-tumor responses in Phase I/Ib, whose platform has drawn Takeda, Bayer and AbbVie as partners, and which raised $150 million in an October 2026 Nasdaq IPO. More features in biotechnology. 19 October 2026

BBNS
Oct 2nd, 2026
Zymeworks completes Theravance deal, adds YUPELRI cash flow and raises 2026 outlook.

Zymeworks completes Theravance deal, adds YUPELRI cash flow and raises 2026 outlook. Posted by Don Miller on Oct 2nd, 2026 Zymeworks (NASDAQ:ZYME) said it has completed its acquisition of Theravance Biopharma, adding the COPD medicine YUPELRI, an acquired research portfolio, collaboration and royalty economics, Irish tax attributes and a commercial organization to its business. Management said the transaction represents an expansion of Zymeworks' strategy beyond its historical focus on research and development catalysts. The company now expects to operate with multiple sources of revenue and operating cash flow, including profit-sharing economics from YUPELRI and royalties associated with ZIIHERA. YUPELRI and commercial operations. YUPELRI is a once-daily nebulized long-acting muscarinic antagonist, or LAMA, for patients with chronic obstructive pulmonary disease who may have difficulty using handheld inhalers. Viatris is responsible for community promotion of the product, while Zymeworks has retained the hospital promotion organization acquired from Theravance. Scott Platshon, Zymeworks' chief business officer, said hospital sales for YUPELRI grew approximately 25% year over year in the second quarter of 2026. He said the hospital channel remains underpenetrated and offers opportunities both to bring new hospital accounts online and to expand use within existing accounts. "The answer is both," Platshon said in response to a question about whether growth is being driven by new accounts or existing hospitals. He noted that gaining hospital formulary access can take from six months to multiple years. Management said approximately 12% to 13% of YUPELRI volume currently comes from the hospital channel. Platshon also said the hospital setting can support community use after patients are discharged, as hospitals, payers and patients may have incentives to maintain treatment with YUPELRI. Zymeworks plans to add Stuart Knight as executive vice president and chief information officer, and Jesse Fecker as vice president of intellectual property. The company also plans to hire an experienced pharmaceutical executive to lead the Theravance commercial operations. Financing structure and expected returns. Zymeworks said its base-case underwriting anticipates a mid-teen internal rate of return over the long term, primarily driven by YUPELRI and with a smaller contribution from VIBATIV, an antibiotic sold by Cumberland. Management said the base case does not assign value to the acquired research portfolio, Irish tax attributes or certain potential milestones and business-development opportunities. The acquisition was financed in part through a $350 million non-recourse, royalty-backed note with OMERS Life Sciences. The financing is secured solely by YUPELRI cash flows, according to the company. YUPELRI is currently generating approximately $60 million in annualized cash flows at current run rates, Zymeworks said. During the note period, OMERS will receive 75% of YUPELRI profit-share cash flows to service interest and principal, while Zymeworks retains the residual economics. After repayment, the remaining cash flows will revert to Zymeworks. Chief Financial Officer Kristin Stafford said the company was not providing guidance on the timing of repayment. Stafford said YUPELRI economics are structured around a 35%/65% profit-sharing arrangement with Viatris. Viatris records 100% of product net sales, while Theravance historically reported net collaboration revenue reflecting its share of profits and losses and shared-cost adjustments. Guidance and capital allocation. Following the acquisition and a $250 million milestone payment triggered by FDA approval of ZIIHERA in gastroesophageal adenocarcinoma on Aug. 25, 2026, Zymeworks issued updated 2026 guidance. The company expects: * Total revenue of $278 million to $292 million. * Adjusted EBITDA of $114 million to $128 million, excluding the impact of future transactions. The company said it will use total revenue and adjusted EBITDA as key measures as it transitions to a business supported by several revenue sources. It expects to provide initial 2027 guidance with its 2026 annual results in the first quarter of 2027. Zymeworks said it may allocate cash flow among wholly owned research programs, acquired research assets, additional acquisitions, royalty streams, commercial assets and share repurchases. Management said it will assess these choices based on risk-adjusted returns, strategic fit and its financial position. The company said it accessed approximately $600 million of non-dilutive financing during 2026 through non-recourse notes, supporting the Theravance transaction and share repurchases. Zymeworks said its last public equity offering was in January 2022 and that it currently has no plans for another equity issuance. R&D portfolio and tax attributes. The acquisition includes an R&D portfolio focused broadly on autoimmune and inflammatory programs, according to management. Zymeworks said it will evaluate internal development, partnerships, licensing and spinout options, but will allocate capital only to programs with clear risk-adjusted value-creation potential. The company also acquired approximately $2.5 billion in Irish tax attributes. Stafford said Zymeworks has assigned no value to those attributes in its base-case return analysis or expected purchase accounting, and will evaluate potential uses involving future Irish revenue, intellectual property structuring, acquisitions or investments involving Irish legal entities. Management said it expects to provide more detail on the acquired research portfolio during an R&D day planned for the first quarter of 2027. Before then, Zymeworks expects phase I optimization data for ZW191 to be presented at ESMO in Madrid on Oct. 24. About Zymeworks (NASDAQ:ZYME). Zymeworks Inc (NASDAQ: ZYME) is a biopharmaceutical company focused on discovering, developing and commercializing engineered antibody-based therapeutics for cancer and other serious diseases. The company's technologies are designed to create bispecific and multispecific antibodies, as well as antibody-drug conjugates that can target tumor cells and deliver therapeutic payloads. Zymeworks' leading product is zanidatamab, marketed in the United States as Ziihera. The bispecific antibody targets two separate sites on the HER2 protein and received U.S.

The Lincolnian Online
Oct 2nd, 2026
Zymeworks completes Theravance deal, adds YUPELRI cash flow and raises 2026 outlook.

Zymeworks completes Theravance deal, adds YUPELRI cash flow and raises 2026 outlook. Zymeworks (NASDAQ:ZYME) said it has completed its acquisition of Theravance Biopharma, adding the COPD medicine YUPELRI, an acquired research portfolio, collaboration and royalty economics, Irish tax attributes and a commercial organization to its business. Management said the transaction represents an expansion of Zymeworks' strategy beyond its historical focus on research and development catalysts. The company now expects to operate with multiple sources of revenue and operating cash flow, including profit-sharing economics from YUPELRI and royalties associated with ZIIHERA. YUPELRI and commercial operations. Discover more Business Analysis Reports Business Strategy Insights Invest in Stocks YUPELRI is a once-daily nebulized long-acting muscarinic antagonist, or LAMA, for patients with chronic obstructive pulmonary disease who may have difficulty using handheld inhalers. Viatris is responsible for community promotion of the product, while Zymeworks has retained the hospital promotion organization acquired from Theravance. Scott Platshon, Zymeworks' chief business officer, said hospital sales for YUPELRI grew approximately 25% year over year in the second quarter of 2026. He said the hospital channel remains underpenetrated and offers opportunities both to bring new hospital accounts online and to expand use within existing accounts. "The answer is both," Platshon said in response to a question about whether growth is being driven by new accounts or existing hospitals. He noted that gaining hospital formulary access can take from six months to multiple years. Management said approximately 12% to 13% of YUPELRI volume currently comes from the hospital channel. Platshon also said the hospital setting can support community use after patients are discharged, as hospitals, payers and patients may have incentives to maintain treatment with YUPELRI. Zymeworks plans to add Stuart Knight as executive vice president and chief information officer, and Jesse Fecker as vice president of intellectual property. The company also plans to hire an experienced pharmaceutical executive to lead the Theravance commercial operations. Financing structure and expected returns. Zymeworks said its base-case underwriting anticipates a mid-teen internal rate of return over the long term, primarily driven by YUPELRI and with a smaller contribution from VIBATIV, an antibiotic sold by Cumberland. Management said the base case does not assign value to the acquired research portfolio, Irish tax attributes or certain potential milestones and business-development opportunities. The acquisition was financed in part through a $350 million non-recourse, royalty-backed note with OMERS Life Sciences. The financing is secured solely by YUPELRI cash flows, according to the company. YUPELRI is currently generating approximately $60 million in annualized cash flows at current run rates, Zymeworks said. During the note period, OMERS will receive 75% of YUPELRI profit-share cash flows to service interest and principal, while Zymeworks retains the residual economics. After repayment, the remaining cash flows will revert to Zymeworks. Chief Financial Officer Kristin Stafford said the company was not providing guidance on the timing of repayment. Stafford said YUPELRI economics are structured around a 35%/65% profit-sharing arrangement with Viatris. Viatris records 100% of product net sales, while Theravance historically reported net collaboration revenue reflecting its share of profits and losses and shared-cost adjustments. Guidance and capital allocation. Following the acquisition and a $250 million milestone payment triggered by FDA approval of ZIIHERA in gastroesophageal adenocarcinoma on Aug. 25, 2026, Zymeworks issued updated 2026 guidance. The company expects: * Total revenue of $278 million to $292 million. * Adjusted EBITDA of $114 million to $128 million, excluding the impact of future transactions. The company said it will use total revenue and adjusted EBITDA as key measures as it transitions to a business supported by several revenue sources. It expects to provide initial 2027 guidance with its 2026 annual results in the first quarter of 2027. Zymeworks said it may allocate cash flow among wholly owned research programs, acquired research assets, additional acquisitions, royalty streams, commercial assets and share repurchases. Management said it will assess these choices based on risk-adjusted returns, strategic fit and its financial position. The company said it accessed approximately $600 million of non-dilutive financing during 2026 through non-recourse notes, supporting the Theravance transaction and share repurchases. Zymeworks said its last public equity offering was in January 2022 and that it currently has no plans for another equity issuance. R&D portfolio and tax attributes. The acquisition includes an R&D portfolio focused broadly on autoimmune and inflammatory programs, according to management. Zymeworks said it will evaluate internal development, partnerships, licensing and spinout options, but will allocate capital only to programs with clear risk-adjusted value-creation potential. The company also acquired approximately $2.5 billion in Irish tax attributes. Stafford said Zymeworks has assigned no value to those attributes in its base-case return analysis or expected purchase accounting, and will evaluate potential uses involving future Irish revenue, intellectual property structuring, acquisitions or investments involving Irish legal entities. Management said it expects to provide more detail on the acquired research portfolio during an R&D day planned for the first quarter of 2027. Before then, Zymeworks expects phase I optimization data for ZW191 to be presented at ESMO in Madrid on Oct. 24. About Zymeworks (NASDAQ:ZYME). Zymeworks Inc (NASDAQ: ZYME) is a biopharmaceutical company focused on discovering, developing and commercializing engineered antibody-based therapeutics for cancer and other serious diseases. The company's technologies are designed to create bispecific and multispecific antibodies, as well as antibody-drug conjugates that can target tumor cells and deliver therapeutic payloads. Zymeworks' leading product is zanidatamab, marketed in the United States as Ziihera. The bispecific antibody targets two separate sites on the HER2 protein and received U.S.

Yahoo Finance
Aug 26th, 2026
SJM raises FY27 outlook to $10.50-$11/share after Q1 beat, ZYME surges on $250M FDA milestone

J.M. Smucker and Zymeworks shares reached 52-week highs on Wednesday following strong corporate developments. Smucker rose 4.1% after reporting first-quarter net sales of $2.2 billion, beating estimates of $2.13 billion. The food company raised its fiscal 2027 adjusted earnings forecast to between $10.50 and $11 per share, up from previous guidance of $9.75 to $10.25 per share. Zymeworks climbed 6%, hitting its highest level in nearly five years. The biotech firm received a $250 million milestone payment after the US Food and Drug Administration approved two Ziihera-based treatments for advanced HER2-positive gastroesophageal cancer. H.C. Wainwright raised Zymeworks' price target to $55 from $51, maintaining a buy rating.