Full-Time

Market Development Manager

West

Posted on 10/31/2025

Omeros

Omeros

201-500 employees

Biopharmaceutical company developing MASP-2 inhibitors

Compensation Overview

$200k - $225k/yr

+ Incentive + Stock Options

United States

In Person

Overnight travel 5-10 days per month.

Category
Sales & Account Management (1)
Required Skills
Branding/Brand Strategy
Requirements
  • Bachelor’s degree in science, business, or marketing
  • 10+ years of experience in the pharmaceutical or biotechnology industry, spanning sales, marketing, or commercial operations
  • Strong background in market development, including previous marketing or field-based marketing experience; a mix of sales and marketing experience is highly preferred
  • At least 5 years of experience in hospital or account-based sales within oncology, stem cell therapy, or related therapeutic areas
  • Proven ability to lead cross-functional projects and drive strategic initiatives
  • Committed to the highest ethical and professional standards
Responsibilities
  • Enabling Launch Excellence: Gather and leverage market insights to ensure Omeros’ innovative complement inhibitor therapies are effectively and safely delivered across various sites of care, while driving a best-in-class customer experience to support successful product launches and market adoption
  • Lead onboarding efforts for accounts within a defined U.S. region, collaborating with internal teams and external stakeholders including clinical staff, department leads, operations, supply chain, and executive leadership
  • Maintain proactive communication with account stakeholders and facilitate connections with Omeros commercial team members throughout the onboarding journey
  • Deliver training on Omeros products and support accounts in building appropriate prescribing and management infrastructure
  • Monitor industry trends in stem cell and post-transplant therapies to inform long-term strategic planning
  • Partner closely with field sales to ensure consistent execution of brand strategies at the healthcare provider level
  • Lead cross-functional launch readiness workshops with Transplant Clinical Account Managers to align on execution strategies and account-specific needs
  • Opinion Leader (OL) Advocacy, Alignment and Development: Cultivate and manage strong relationships with national and regional Opinion Leaders in transplant, hematology/oncology, and nephrology
  • Partner with Marketing to drive OL involvement in advisory boards, training, speaking engagements, and major events
  • Execute targeted OL engagement plans in collaboration with internal stakeholders
  • Represent the company at key medical and scientific conferences (e.g., ASTCT, ASH) to build visibility and engagement
  • Speaker Identification and Training: Collaborate cross-functionally to identify and evaluate promotional speaker candidates
  • Oversee speaker contracting, training, and ongoing education
  • Develop and implement the regional speaker engagement plan, ensuring efficient management of the speaker bureau
  • Attend and support local, regional, and national speaker programs
  • Brand Optimization and Program Execution: Track and analyze field marketing promotional spend to support strategic decisions and ensure alignment with customer and patient needs
  • Develop metrics to assess ROI on marketing investments and activities
  • Provide timely, strategic evaluations of speaker and program effectiveness
  • Collaborate with brand and sales leadership, and speakers to gather feedback and refine promotional content and sales/educational materials
  • Oversee onboarding processes, ensuring compliance with Omeros’ regulatory and legal standards
Desired Qualifications
  • Proven ability to build and maintain strong relationships with cross-functional teams—including sales, market access, and senior leadership—to drive alignment and deliver impactful marketing initiatives
  • A results-oriented mindset with a strong work ethic and personal accountability for meeting deadlines, and business objectives
  • Outstanding written and verbal communication skills
  • Excellent analytical, planning, and organizational skills, with the ability to interpret market data
  • Willingness to travel overnight approximately 5 to 10 days per month, including some weekends

Omeros develops therapeutics that target the immune system, focusing on complement pathway biology to treat immunologic and CNS disorders. It manages the full drug process from discovery to commercialization through a vertically integrated model. The lead candidate narsoplimab blocks MASP-2 in the lectin pathway to reduce inflammation without impairing the classical pathway, with other programs targeting MASP-3 and long-acting MASP-2 inhibitors. The goal is to address unmet medical needs by advancing complement-targeted therapies and expanding its pipeline and collaborations.

Company Size

201-500

Company Stage

IPO

Headquarters

Charlottesville, Virginia

Founded

1994

Simplify Jobs

Simplify's Take

What believers are saying

  • Novo Nordisk deal yields $340M upfront plus $2.1B milestones.
  • YARTEMLEA ships commercially to 80 high-volume US transplant centers.
  • $171.8M cash supports positive cash flow by 2027.

What critics are saying

  • EMA delays YARTEMLEA approval past mid-2026, blocking Europe revenue.
  • Novo terminates zaltenibart milestones after Phase III PNH failure.
  • OMS1029 Phase II fails efficacy, halting MASP-2 pipeline.

What makes Omeros unique

  • YARTEMLEA inhibits MASP-2, targeting lectin pathway uniquely.
  • First FDA-approved therapy for TA-TMA in adults and pediatrics.
  • Vertically integrated from discovery to commercialization since 1994.

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Benefits

Remote Work Options

Flexible Work Hours

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

2%
Yahoo Finance
Apr 1st, 2026
Omeros secures up to $2.1B from Novo Nordisk sale, targets cash flow positive in 2027

Omeros Corporation reported its Q4 2025 earnings, highlighting its transition to a commercial-stage company following FDA approval of YARTEMLEA, the first treatment for TA-TMA. The company sold zaltenibart to Novo Nordisk for up to $2.1 billion, using proceeds to fully repay senior secured debt. Management expects YARTEMLEA to achieve financial self-sustainability within 2026 and company-wide positive cash flow in 2027. The commercial strategy targets 80 high-volume transplant centres representing 80% of the US market. A European regulatory decision is anticipated by mid-2026. Reported net income included a $136 million non-cash charge on embedded derivatives, driven by a 319% stock price increase in Q4. The company expects $100 million in near-term milestones from Novo Nordisk and is advancing its MASP-2 pipeline, including Phase II candidate OMS1029.

Yahoo Finance
Apr 1st, 2026
Omeros secures $2.1B Novo Nordisk deal and FDA approval for YARTEMLEA, swings to $86.5M Q4 profit

Omeros Corp has reported a net income of $86.5 million for Q4 2025, reversing a $30.9 million loss in the previous quarter, driven by a $237.6 million gain from its zaltnibart transaction with Novo Nordisk. The company closed an asset purchase and license deal with Novo Nordisk valued at up to $2.1 billion, including a $240 million upfront payment. This helped strengthen Omeros's balance sheet, with cash and investments reaching $171.8 million as of 31st December 2025. The FDA approved YARTEMLEA, the first treatment for TA-TMA, priced at approximately $36,000 per vial. The company has begun early sales deployment but has not provided revenue guidance due to the launch's early stage. Omeros has reduced outstanding debt to $70.8 million in convertible notes.

WDFX-TV
Mar 21st, 2026
Omeros announces upcoming presentation at EBMT 2026 highlighting advances in TA-TMA Treatment.

Omeros announces upcoming presentation at EBMT 2026 highlighting advances in TA-TMA Treatment. * 2 hrs ago Omeros Corporation (NASDAQ: OMER) today announced that it will host an industry session at the 52nd Annual Meeting of the European Society for Blood and Marrow Transplantation (EBMT) on March 22, 2026, from 2:30pm - 4pm CET in Madrid, Spain. The session, titled "Advances in TA-TMA Treatment: Evaluating the Role of a Novel Targeted Therapy," will be co-chaired by Rafael Duarte, MD, PhD, Hospital Universitario Puerta de Hierro Majadahonda, and Mohamad Mohty, MD, PhD, Hôpital Saint-Antoine, AP-HP, and will feature speakers Miguel-Angel Perales, MD, Memorial Sloan Kettering Cancer Center, and Michelle L. Schoettler, MD, MS, Children's Healthcare of Atlanta. The EBMT Annual Meeting is a key event for professionals in transplantation and cellular therapy, bringing together stakeholders from around the world. About Omeros Corporation Omeros is an innovative, commercial-stage biotechnology company that discovers and develops first-in-class protein and small-molecule therapeutics for large-market and orphan indications, with particular emphasis on complement-mediated diseases, cancers, and addictive or compulsive disorders. Omeros' lead lectin pathway inhibitor YARTEMLEA(R)(narsoplimab-wuug), which inhibits the pathway's effector enzyme MASP-2, is FDA-approved and commercially available in the U.S. for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA) in adult and pediatric patients aged two years and older. A marketing authorization application for YARTEMLEA in TA-TMA is currently under review at the European Medicines Agency. OMS1029, Omeros' long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials. Under a recently announced asset purchase and licensing agreement, Novo Nordisk acquired global rights to zaltenibart (formerly OMS906), a MASP-3 inhibitor in clinical development for PNH and other alternative pathway indications, along with associated intellectual property and related assets. Omeros' pipeline also includes OMS527, a phosphodiesterase 7 inhibitor in clinical development for cocaine use disorder that is fully funded by the National Institute on Drug Abuse, as well as a growing portfolio of novel molecular and cellular oncology programs. For more information about Omeros and its programs, visit www.omeros.com.

Business Wire
Jan 27th, 2026
Omeros ships first commercial orders of YARTEMLEA for stem cell transplant complication

Omeros Corporation has completed its first commercial shipments of YARTEMLEA (narsoplimab-wuug), with transplant centres beginning orders immediately. Both adult and paediatric patients with stem cell transplant-associated thrombotic microangiopathy (TA-TMA) are now receiving treatment in hospital and outpatient settings. YARTEMLEA is the first and only approved therapy for TA-TMA, a potentially fatal complication of stem cell transplantation. The drug received FDA approval on 23 December 2025 for use in adults and children aged two years and older. TA-TMA develops in up to 56% of allogeneic transplant recipients, according to recent studies. Approximately 30,000 allogeneic transplants are performed annually in the United States and Europe. A marketing authorisation application is under review by the European Medicines Agency, with a decision expected in mid-2026.

GlobalData
Oct 16th, 2025
Novo Nordisk snaps up Omeros' rare disease asset for up to $2.1bn

Novo Nordisk snaps up Omeros' rare disease asset for up to $2.1bn. Novo Nordisk will now run a Phase III trial for zaltenibart in the rare blood disorder, PNH. Danish pharma giant Novo Nordisk has inked a definitive deal with Omeros Corporation to acquire its late-stage-ready rare disease asset, zaltenibart. By selling the rights to the monoclonal antibody (mAb), which demonstrated potential in a Phase II trial in blood disorder paroxysmal nocturnal haemoglobinuria (PNH), Omeros will pocket $340m in upfront and short-term milestone payments. The biopharma is also eligible to receive up to $2.1bn in development and commercial milestone payments from Novo Nordisk, depending on how the drug performs in upcoming Phase III trials in PNH. These studies will be initiated and funded by Novo Nordisk. Formerly known as OMS906, zaltenibart was due to enter Phase III clinical trials under Omeros' name, but the company later pressed pause on the drug's late-stage development. This came after Omeros forecasted a "ramp up in spending" on these studies, which led the biopharma to "prioritise" the use of capital currently available to it. Zaltenibart's financial performance could bode well for the rest of Omeros' pipeline, according to investor reaction. The company's stock value shot up more than 180% after the news debuted, going from $4.10 at market close on 14 October to $11.59 at market open on 15 October. Novo's choice to purchase zaltenibart will bolster the company's rare blood disease pipeline, which currently includes five drugs in Phases I to III. This includes erythrocyte pyruvate kinase (PKR) activator etavopivat, which the pharma obtained through its acquisition of Forma in 2022 and is now in Phase III trials for sickle cell disease. US tariffs are shifting - will you react or anticipate? Don't let policy changes catch you off guard. Stay proactive with real-time data and expert analysis. Zaltenibart's future potential. Zaltenibart works by inhibiting the mannan-binding lectin-associated serine protease-3 (MASP-3), a complement system enzyme that is key to activating the alternative pathway. According to Sir Peter Lachmann, Emeritus Sheila Joan Smith Professor of Immunology at the University of Cambridge, MASP-3 inhibitors such as zaltenibart could have "important advantages relative to a complement 5 (C5) inhibitor," for treating PNH. Lachmann noted that this was likely due to zaltenibart's ability to block both intra- and extravascular haemolysis, which he said C5 inhibitors cannot achieve. As a result, zaltenibart could take a chunk of the PNH market if approved. The indication is currently dominated by C5 inhibitors such as AstraZeneca's Soliris (eculizumab) and Ultomiris (ravulizumab). However, the recent market debut of Novartis' Fabhalta (iptacopan) could be a spanner in the works for intravenous (IV) therapies like zaltenibart, as the drug is orally administered - enhancing patient convenience. Outside of PNH, Omeros has previously touted the potential of the mAb in other rare blood and kidney disorders. Following its acquisition of zaltenibart, Novo Nordisk will explore further development opportunities for the drug in a "range" of undisclosed indications. Give your business an edge with our leading industry insights. Pharmaceutical Technology Excellence Awards - The benefits of entering. Gain the recognition you deserve! The Pharmaceutical Technology Excellence Awards celebrate innovation, leadership, and impact. By entering, you showcase your achievements, elevate your industry profile, and position yourself among top leaders driving pharmaceutical advancements. Don't miss your chance to stand out - submit your entry today!

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