Adaptive Biotechnologies

👥 501-1000💰 $125,000,000 Post-IPO Debt over 2 years ago🫂 Last layoff almost 3 years agoBiotechnology Therapeutics Health Care📈 Public Company

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Adaptive Biotechnologies: Revolutionizing Immune-Driven Medicine Adaptive Biotechnologies is a publicly traded company (NASDAQ: ADPT) pioneering the field of immune-driven medicine. Our flagship product, clonoSEQ, is an FDA-authorized test for detecting and monitoring minimal residual disease (MRD) in patients with select blood cancers, significantly impacting cancer treatment decisions. We leverage the power of the adaptive immune system to transform disease diagnosis and treatment, setting a new standard for precision medicine. Our work relies on a robust technological foundation. We utilize a modern tech stack including Amazon Web Services, Microsoft Azure, and Cloudflare, enabling a scalable and secure infrastructure for our innovative bioinformatics pipelines. Our engineering culture embraces automation (via Ansible) and DevOps practices, ensuring efficient and high-quality software delivery. We prioritize collaboration and innovation, fostering a dynamic environment where engineers directly contribute to improving patient outcomes. Adaptive Biotechnologies offers a remote-friendly work environment, allowing talented individuals to contribute from various locations. We are committed to building diverse, equitable, and inclusive teams and pride ourselves on a culture of collaboration and continuous learning. Our continued growth and significant funding demonstrate our commitment to advancing immune medicine and improving patient lives. Join us in shaping the future of healthcare. With over 500 employees and continued expansion, Adaptive Biotechnologies offers numerous growth opportunities in a fast-paced, impactful environment.

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Jobs at this company:

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🔥 Senior Director, Regulatory Affairs

Posted about 1 month ago

💸 204300.0 - 306500.0 USD per year

🔍 Diagnostics, medical device or life sciences technology

🔧 Requirements

BA/BS undergraduate degree in life sciences; MS, PhD or relevant advanced degree preferred.
17+ years of progressive management experience in global regulatory affairs in a diagnostic, medical device or life sciences company.
In vitro diagnostics (IVD) experience required.
Experience with regulatory submissions in hematology, oncology, immunology or similar fields.
Extensive knowledge of compliance requirements and product development lifecycle.

💡 Responsibilities

Provide management and leadership to the Regulatory Affairs team in developing regulatory strategies.
Lead planning for regulatory agency meetings and represent Adaptive during negotiations.
Monitor and communicate emerging regulations and assess their impact on products.
Prepare and oversee regulatory submissions to the FDA and international agencies.
Identify regulatory risks related to clinical development and develop mitigation strategies.
Collaborate cross-functionally to ensure product compliance and market access.

Posted about 1 month ago

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🔥 Medical Science Liaison / Senior Medical Science Liaison (West)

Posted 2 months ago

🧭 Full-Time

💸 161500.0 - 242300.0 USD per year

🔍 Immune Medicine

🔧 Requirements

Doctorate-level degree (PhD, PharmD, MD, DNP) or advanced professional degree with significant clinically relevant experience (PA, NP) required.
Prior Medical Science Liaison experience preferred.
Working knowledge of regulatory guidance and reporting requirements required.
Strong presentation skills including excellent verbal and written communication.
Relevant industry and clinical therapeutic-specific experience.
Existing relationships with academic institutions and key opinion leaders preferred.
Demonstrated understanding of clinical trial management.
Previous medical device/diagnostic/pharmaceutical industry experience preferred.
Experience with regulatory compliance requirements (ISO, CLIA, CAP, etc.) preferred.

💡 Responsibilities

Develop and maintain significant scientific relationships with Key Opinion Leaders (KOLs) and other healthcare providers.
Serve as a trusted clinical education/information subject matter expert to healthcare providers.
Provide feedback and insights from interactions with healthcare providers.
Coordinate local and regional investigator sponsor trial initiatives.
Manage IST milestones and objectives.
Report on scientific sessions at congresses.
Respond to and document unsolicited requests for scientific information.
Assist with training and provide clinical input to internal functions.
Support content development and delivery of clinical presentations at Advisory Boards.
Work closely with other field-based teams and HQ staff.

Posted 2 months ago

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🔥 Senior Product Marketing Manager

Posted 2 months ago

📍 United States

🧭 Full-Time

💸 143200.0 - 214800.0 USD per year

🔍 Healthcare / Immune Medicine

🔧 Requirements

Bachelor’s degree plus 12 years of related experience or master’s degree plus 10 years of related experience.
Minimum of 8 years in a Marketing team within a highly regulated healthcare environment.
At least 3 years of experience in oncology/hematology/immunology.
Proven success in complex marketing strategy execution, encompassing digital promotion and market research.
Significant experience managing external vendors and delivering projects on-time and within budget.
Experience in cross-functional product launch planning.
Ability to analyze scientific publications and translate clinical data into promotional narratives.
Strong interpersonal skills and ability to communicate effectively with diverse stakeholders.
Self-starter with project leadership abilities, capable of working both autonomously and collaboratively.
Excellent communication and presentation skills.

💡 Responsibilities

Partner with clonoSEQ Marketing leadership to develop impactful annual business plans, including budgets and tactical plans.
Lead patient marketing tactical efforts to educate patients on the clinical value of clonoSEQ.
Collaborate with Sales, Medical Affairs, Customer Operations, and other stakeholders to execute strategies for new product offerings.
Manage agency partners on marketing collateral projects, providing strategic direction and feedback.
Establish and socialize key patient audience KPIs to ensure alignment with business objectives.
Manage all projects and external vendors within specified budgets and timelines.
Work with Sales Training for optimal rollout of initiatives and participate in field activities.
Maintain a broad understanding of market landscape and industry trends.

Project ManagementData AnalysisContent creationCross-functional collaborationMarket ResearchMarketingStakeholder managementDigital MarketingBudget management

Posted 2 months ago

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🔥 Senior Legal Specialist

Posted 3 months ago

📍 Greater Seattle area

🧭 Full-Time

💸 100600.0 - 150800.0 USD per year

🔍 Bio/pharma/medical device/diagnostics

🔧 Requirements

Bachelor’s degree in law, public policy, marketing, business, finance, or related discipline preferred.
5 years of experience in legal, policy, auditing, training, or related disciplines, preferably in the bio/pharma/medical device/diagnostics industry.
In-depth knowledge of the legal and regulatory environment, including privacy and employment law.
Strong verbal and written communication skills for synthesizing complex information.
Ability to work in fast-paced conditions and demonstrate good judgment.
Proven effectiveness in developing scalable processes for organizational efficiency.
Excellent project management skills for prioritizing multiple tasks.
Proficiency in Microsoft Office and legal operations technologies.
Preference for candidates with privacy and employment matter experience.
Specialist certification (CIPP, SHRM) is a plus.

💡 Responsibilities

Manage operational relationships with outside counsel and legal service providers.
Assist in negotiations and enforce engagement agreement terms with law firms.
Oversee legal technology services and manage procurement and implementation.
Manage registered agent and corporate filings vendor.
Support administrative activities of the legal department, including investigations and incident management.
Analyze processes for law and compliance management to promote efficiency.
Ensure compliance with local CLE and registration requirements for attorneys.
Develop and oversee department KPIs for accurate and timely reporting.
Support strategic ad hoc projects and initiatives as needed.

Project ManagementData AnalysisComplianceProcess improvement

Posted 3 months ago

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🔥 Medical Science Liaison / Senior Medical Science Liaison (Midwest)

Posted 3 months ago

🧭 Full-Time

💸 161500.0 - 272300.0 USD per year

🔍 Immune medicine

🔧 Requirements

Doctorate-level degree (PhD, PharmD, MD, DNP) or advanced professional degree with significant clinically relevant experience (PA, NP) required.
4+ years relevant industry and/or hematology/oncology disease experience required.
Strong presentation skills including excellent verbal and written communication.
In-depth scientific and/or therapeutic knowledge required.
Existing relationships with key opinion leaders and affiliated institutions required.
Demonstrated understanding of clinical trial management.
Working knowledge of regulatory guidance and reporting requirements.
Exceptional organizational and time management skills.
Strong interpersonal skills and demonstrated ability to work effectively in a cross-functional team.

💡 Responsibilities

Develop and maintain scientific relationships with Key Opinion Leaders (KOLs) and other healthcare providers in academic and community settings.
Serve as a trusted clinical education/information subject matter expert to healthcare providers on implementing MRD in patient management.
Provide internal teams with feedback and insights from interactions and discussions with healthcare providers.
Coordinate local and regional investigator sponsor trial initiatives.
Manage IST milestones and objectives.
Report on scientific sessions at congresses and respond to unsolicited requests for scientific information.
Support content development and delivery of clinical presentations at Advisory Boards.
Collaborate closely with field-based teams and HQ staff to timely respond to information requests.
Lead multiple complex projects requiring understanding of current business trends and industry practices.

Posted 3 months ago

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