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Manager Program Biotech Jobs in Seattle, WA (NOW HIRING)

Senior Project Manager

Redmond, WA ยท On-site

$100 - $160/hr

... in biotech, biopharma, or related life sciences industry. * 5+ years of project or program management experience supporting drug discovery and/or development programs. * Demonstrated experience ...

Quality Assurance Manager

Redmond, WA ยท On-site

$120 - $160/hr

Biotechnology What You'll Do: * Maintain and improve the Quality Management System (QMS) across ... Referral Bonus Programs * Certification and training opportunities Note: Any pay ranges displayed ...

New

LNP Lab Technician

Redmond, WA ยท On-site

$55K - $65K/yr

About GenScript Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation ... Inventory Management: Keep track of inventory using our management system, and proactively order ...

Showing results 21-40

Manager Program Biotech information

See Seattle, WA salary details

$43.8K

$122.3K

$178.7K

How much do manager program biotech jobs pay per year?

As of Aug 20, 2026, the average yearly pay for manager program biotech in Seattle, WA is $122,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $150,800.00 per year, depending on experience, location, and employer.

What does a manager program biotech do?

A Manager Program Biotech oversees and coordinates biotechnology projects within an organization. They are responsible for planning, executing, and monitoring projects to ensure they meet scientific, regulatory, and business objectives. This role involves leading cross-functional teams, managing budgets and timelines, and communicating progress to stakeholders. Managers in this position often work closely with research scientists, regulatory affairs, and business development teams to bring biotech products from concept to market.

What are the key skills and qualifications needed to thrive as a manager program biotech?

To thrive as a Manager Program Biotech, you need a strong background in life sciences, project management experience, and typically an advanced degree such as an MS or PhD in biotechnology or a related field. Familiarity with project management software, regulatory compliance systems, and knowledge of drug development processes are essential. Outstanding leadership, communication, and problem-solving skills set exceptional candidates apart in this role. These competencies ensure effective coordination of complex projects, regulatory adherence, and successful cross-functional team management in a rapidly evolving industry.

What are some typical challenges faced by a manager program biotech, and how can they be addressed?

A Manager Program in biotech often encounters challenges such as coordinating multidisciplinary teams, managing complex project timelines, and navigating shifting regulatory requirements. Effective communication and proactive risk management are crucial to address these issues. Building strong relationships with stakeholders and fostering a collaborative team environment can also help ensure project milestones are met while maintaining compliance with industry standards.

What is the difference between Manager Program Biotech vs Project Coordinator Biotech?

AspectManager Program BiotechProject Coordinator Biotech
Required CredentialsBachelor's/Master's in Life Sciences, Project Management certification often preferredBachelor's in Life Sciences or related field, PMP or similar certification beneficial
Work EnvironmentOversees multiple projects, manages teams, strategic planningSupports project teams, coordinates activities, tracks project progress
Employer & Industry UsageBiotech companies, pharmaceutical firms, research organizationsBiotech firms, research labs, clinical trial organizations

The Manager Program Biotech typically holds a higher level of responsibility, overseeing multiple projects and managing teams, whereas the Project Coordinator Biotech focuses on supporting project execution and coordination. Both roles require similar educational backgrounds and certifications, but differ in scope and leadership responsibilities.

Infographic showing various Manager Program Biotech job openings in Seattle, WA as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $122,293 per year, or $58.8 per hour.

Senior Project Manager

Systimmune

Redmond, WA โ€ข On-site

$100 - $160/hr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days ago


Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using established drug development platforms, focusing on biโ€‘specific, multiโ€‘specific antibodies, and antibodyโ€‘drug conjugates (ADCs). With multiple assets in various stages of clinical trials for solid tumor and hematologic indications, SystImmune also maintains a robust preclinical pipeline of potential cancer therapeutics in the discovery and INDโ€‘enabling stages.

We are seeking a Senior Project Manager, R&D to support crossโ€‘functional planning and execution for oncology biologics programs from early discovery through INDโ€‘enabling activities and IND submission. This role will partner closely with Research, Translational Sciences, Nonclinical, Regulatory, Clinical Pharmacology, and external partners to drive an integrated development strategy, stageโ€‘appropriate planning, risk management, and operational execution.

Key Responsibilities
  • Lead crossโ€‘functional project planning and execution for oncology biologics programs spanning target/lead discovery, candidate selection, INDโ€‘enabling studies, CMC development, and IND submission.
  • Build, maintain, and drive integrated project plans, timelines, milestones, scenarios, and critical path analyses across multiple functional areas.
  • Partner with program leaders and functional heads to define development strategy, key objectives, deliverables, governance milestones, and resource assumptions.
  • Facilitate crossโ€‘functional team meetings, subโ€‘team meetings, and governance reviews; document decisions, action items, risks, and next steps.
  • Identify interdependencies, operational risks, and potential bottlenecks early; drive mitigation plans and upscale issues appropriately.
  • Ensure alignment across Research, Nonclinical, CMC, Regulatory, Clinical, Biomarker/Translational, Quality, and partner organizations.
  • Drive program team preparedness for major stage gates, including candidate nomination, development candidate selection, INDโ€‘enabling study initiation, and IND submission.
  • Support budget planning, resource tracking, and external partner/CRO coordination as needed.
  • Develop concise, decisionโ€‘oriented communications for senior leadership, governance bodies, and key stakeholders.
  • Track progress against program goals and proactively highlight deviations, tradeโ€‘offs, and decision needs.
  • Promote disciplined program management practices, clear accountability, and efficient team operations.
  • Contribute to portfolio planning and crossโ€‘program prioritization discussions where appropriate.
  • Help apply and improve R&D project management tools, templates, dashboards, and best practices.
  • Drive scalable adoption of AIโ€‘enabled and digital program management practices, including automation, dashboards, AIโ€‘assisted synthesis, standardized workflows, and dataโ€‘driven reporting while ensuring human oversight, data integrity, and compliance.
Required Qualifications
  • Bachelorโ€™s degree in life sciences, biomedical sciences, chemistry, engineering, or related field.
  • 8+ years of relevant experience in biotech, biopharma, or related life sciences industry.
  • 5+ years of project or program management experience supporting drug discovery and/or development programs.
  • Demonstrated experience managing biologics programs in oncology or closely related therapeutic areas.
  • Strong understanding of drug development from discovery through IND, including: discovery research and candidate selection, INDโ€‘enabling toxicology and pharmacology, CMC and analytical development for biologics, regulatory documentation and IND submission processes.
  • Proven ability to lead highly matrixed, crossโ€‘functional teams without direct authority.
  • Excellent communication, facilitation, organizational, and stakeholder management skills.
  • Strong problemโ€‘solving abilities with demonstrated experience managing complex timelines, dependencies, and risks.
  • Experience preparing executiveโ€‘level presentations, status reports, and governance materials.
Preferred Qualifications
  • Advanced degree (MS, PhD, PharmD, or MBA) in a relevant scientific or business discipline.
  • Experience with monoclonal antibodies, bispecifics, ADCs, or other complex biologic modalities in oncology.
  • Mandarinโ€‘English bilingual ability.
  • PMP or related project management certification is a plus and biotherapeutics life cycles.
  • Experience in a fastโ€‘paced, innovationโ€‘driven biotech environment.
Core Competencies
  • Strategic thinking with strong operational execution.
  • Crossโ€‘functional leadership and influence.
  • Decision facilitation and issue resolution.
  • Planning discipline and attention to detail.
  • Agility in a dynamic R&D environment.
  • Strong sense of ownership and accountability.
Success in this role will be defined by the ability to:
  • Keep complex oncology biologics programs aligned and moving forward from discovery to IND.
  • Create clarity across scientific and development teams around priorities, timelines, and decisions.
  • Anticipate risks and dependencies before they become delays.
  • Enable efficient governance and highโ€‘quality decisionโ€‘making.
  • Build trust across functions as a strategic and operational partner.
Position Type/Expected Hours of Work
  • May need to work outside of standard working hours at times.
  • This role is currently working onsite and is expected to work onsite during working hours, with flexibility to work start time. The work location for this role is in Redmond, WA.
Compensation and Benefits

The expected base salary range for this position is $100,000 - $160,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidateโ€™s qualifications, experience, and skills. While most offers typically fall within the low to midโ€‘point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.

SystImmune offers a comprehensive benefits package, including: 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match up to 3% and a vesting schedule of 5 years, 15 PTO days per year, sick leave, 11 paid holidays and additional benefits.

We offer an opportunity for you to learn and grow while making significant contributions to the companyโ€™s success.

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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