artiva biotherapeutics jobs
Manager, Biomarker Operations
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $130,000 - $142,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- Reporting to the Senior Manager, Biomarker Operations, the Manager, Biomarker Operations is responsible for managing operational aspects of the clinical…
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Principal Scientist, Analytical Development
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $170,000 - $185,000 a year
- Full-time
- 401(k)
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- Paid time off
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- Dental insurance
- Flexible spending account
- The incumbent will lead and set the strategic direction for the cell potency analytical development team to develop and optimize cell-based assays to support…
Contract Manager
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $122,000 - $145,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
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- The Contract Manager, reporting to the Vice President, General Counsel & Corporate Secretary, is responsible for managing all aspects of Artiva’s contract…
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Associate II, Quality Control Biology
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $79,000 - $91,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- Artiva Biotherapeutics is seeking a skilled and motived QC Associate II, QC Biology who will be reporting to the Senior Manager, Quality Control.
Supervisor, Quality Control Biology
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $110,000 - $135,000 a year
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- 401(k)
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- Artiva Biotherapeutics is seeking a skilled and motivated Quality Control Supervisor who will be reporting to the Senior Manager, Quality Control.
Senior Associate, QA Compliance
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $99,000 - $120,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- This position is responsible for Quality Assurance Compliance activities supporting deviations, CAPAs, change control, and product releases.
Manager, Materials Management Buyer/Planner
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $130,000 - $145,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- The Supply Chain Buyer/Planner is responsible for leading end-to-end inventory and materials management in support of a GMP-regulated (and non-GMP) biologics/…
Director, Corporate Development & Strategy
Easily applyArtiva BiotherapeuticsHybrid work in San Diego, CA 92121- $200,000 - $230,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- The Director, Corporate Development & Strategy is a senior, cross-functional role responsible for shaping and advancing Artiva’s long-range corporate strategy…
Senior Manager, MSAT
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $150,000 - $165,000 a year
- Full-time
- 401(k)
- Health insurance
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- These functions will be executed following standard operating procedures and batch records in accordance with FDA and EU requirements and current Good…
- Artiva BiotherapeuticsSan Diego, CA 92121
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- Vision insurance
- Dental insurance
- Flexible spending account
- Artiva Biotherapeutics seeks a skilled and motivated QC Associate II or III for Environmental Monitoring (EM), to support the Quality Control environmental…
Senior Manager / Associate Director, CMC Project Management - Process Development & Validation
Easily applyArtiva BiotherapeuticsHybrid work in San Diego, CA 92121- $155,000 - $190,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
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- Flexible spending account
- We are seeking an experienced CMC Project Management professional to lead the planning and execution of our process characterization and Process Performance…
- Artiva BiotherapeuticsSan Diego, CA 92121
- $130,000 - $180,000 a year
- Full-time
- 401(k)
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- Flexible spending account
- We are seeking a Clinical Project Manager to drive cross-functional planning, tracking, and operational integration across clinical-stage programs.
- Artiva BiotherapeuticsSan Diego, CA 92121
- $205,000 - $268,000 a year
- Full-time
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- The Director / Senior Director of Regulatory Operations is responsible for building, leading, and scaling the regulatory operations function across Artiva’s…
Senior Associate, Quality Control, Raw Materials
Easily applyArtiva BiotherapeuticsSan Diego, CA 92121- $96,000 - $110,000 a year
- Full-time
- Artiva Biotherapeutics is seeking a skilled and motived Senior Quality Control Associate who will be reporting to the Sr. Manager, Quality Control of Raw…
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Job Post Details
Manager, Biomarker Operations - job post
Job details
Pay
- $130,000 - $142,000 a year
Job type
- Full-time
Benefits
Pulled from the full job description
- 401(k)
- Health insurance
- Paid time off
- Vision insurance
- Dental insurance
- Flexible spending account
- Life insurance
Full job description
About Artiva:
We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.
For more information, visit www.artivabio.com.
Job Summary:
Reporting to the Senior Manager, Biomarker Operations, the Manager, Biomarker Operations is responsible for managing operational aspects of the clinical biomarker projects. This position will be responsible for managing the biomarker operation of Artiva’s clinical studies by coordinating sample-related operations with Clinical Operations, contract executions, and communication between the Translational Science group with external contract research organizations (CRO) and internal lab personnel. The successful candidate will have strong communication and project management skills. Understanding and experience with drug development and clinical trial process is a prerequisite for this position.
Duties/Responsibilities:
- Oversee day-to-day biomarker operations of Artiva’s clinical trials including but not limited to execution of biomarker operations with external vendors, ensuring CROs meet all key deliverables and timelines
- Working closely with the translational leads, manages documentation and performance of biomarker assays conducted at CROs, ensures timely delivery of high-quality biomarker data, and supports CRO audits
- Ensures timely collection kit preparation and sample testing database builds including review of required documentation
- Works with Clinical Operations and CRO to prepare for site activations including preparation of training materials
- Manages collection kit logistics, sample inventory, and sample testing at CROs; tracks and follows up on discrepancies and missing information
- Coordinates shipping and testing scheduling with central lab or 3rd party vendors
- Contributes to data transfer specifications review and implementation
- Assist the internal biomarker laboratory with sample shipping and receiving
- Contributes to translational logistics meetings
Requirements:
Must thrive working in a fast-paced innovative environment while remaining flexible, proactive, and efficient. Excellent communication, project management and interpersonal skills. Able to develop important relationships with key internal stakeholders and external entities.
- Bachelor’s or Master's degree in biology, immunology, or related fields and/or project management experience is required with a minimum of 6 - 8 years’ experience within the biotechnology or pharmaceutical industry
- Demonstrated experience of managing biomarker sample operation of clinical trials, working with CROs to execute biomarker study plan.
- Excellent communication skills, verbal and written
- Understanding and experience with drug development and clinical trial process
Competencies
- Time Management
- Risk Management
- Operations Management
- Finance
- Business Planning
- Implementing Plans
- Analysis and Reporting Negotiation
Attributes
- Honesty/Integrity
- Communication skills
- Self-starter
- Forward thinking
- Creative/imaginative
- Confident
- Self-controlled
- Intuitive
- Positive
- Committed
- Ambitious/driven
- Agile
- Collaborative
- Transparent
In addition to a great culture, we offer:
- A beautiful facility
- An entrepreneurial, highly collaborative, and innovative environment
- Comprehensive benefits, including:
- Medical, Dental, and Vision
- Group Life Insurance
- Long Term Disability (LTD)
- 401(k) Retirement Plan
- Employee Assistance Program (EAP)
- Flexible Spending Account (FSA)
- Paid Time Off (PTO)
- Company paid holidays, including the year-end holiday week
- Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.
If all this speaks to you, come join us on our journey!
Base Salary: $130,000 - $142,000. Exact compensation may vary based on skills and experience.