What are the responsibilities and job description for the Manager / Senior Manager, Clinical Project Management position at Artiva Biotherapeutics?
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:
We are seeking a Clinical Project Manager to drive cross-functional planning, tracking, and operational integration across clinical-stage programs.
This role will serve as a central coordinator across all functions contributing to the development program to ensure alignment on timeline maintenance, risk identification, deliverables, and development milestones. This role is focused on cross-functional program integration, tracking and integration, and organizational alignment.
The ideal candidate combines strong cross functional understanding with program-level thinking and detailed tracking and planning skills in a fast-paced, highly collaborative biotech environment
Duties/Responsibilities:
Timeline Tracking and Integration
Base Salary: $130,000 - $180,000. Exact compensation may vary based on level, skills and experience
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:
We are seeking a Clinical Project Manager to drive cross-functional planning, tracking, and operational integration across clinical-stage programs.
This role will serve as a central coordinator across all functions contributing to the development program to ensure alignment on timeline maintenance, risk identification, deliverables, and development milestones. This role is focused on cross-functional program integration, tracking and integration, and organizational alignment.
The ideal candidate combines strong cross functional understanding with program-level thinking and detailed tracking and planning skills in a fast-paced, highly collaborative biotech environment
Duties/Responsibilities:
Timeline Tracking and Integration
- Responsible for creating, maintaining and communicating cross-functional development project management plans at the task, study and molecule levels
- Responsible for producing cross functional Project Management tools/visuals/GANTS as required in support of the development team in industry standard software packages
- Communicating changes, impacts and potential mitigations across the development team and working to align the cross functional team on best path forward
- Support to the finance organization regarding timeline models, changes, and Financial Planning and Analysis integration.
- Support communication across internal teams and external stakeholders
- Identify, assess, and track cross-functional risks and dependencies across the development team space.
- Communicate to higher organizational structures status, timeline changes and impacts to cross functional deliverables to support mitigation planning.
- Develop and maintain the cross-functional risk register for the development team.
- Ensure timely tracking and modeling of the impact of critical risks impacting program timelines, quality, or strategic milestones
- Support leadership governance activities through preparation of timeline models and scenarios in support of risk assessments. materials.
- Develop and maintain dashboards to support development team in data tracking and communication to Senior Management
- Prepare clear, concise program updates for cross-functional teams and leadership
- Ensure consistent reporting across ongoing clinical studies
- Support cross-functional governance meetings, including agenda setting, materials preparation, decision tracking, and follow-up actions
- Ensure decisions, actions, and dependencies are clearly documented and tracked
- Drive accountability across teams for agreed-upon deliverablesRequirements:
- Bachelor’s degree in life sciences or related field
- 5–8 years of experience of program management in biotechnology, pharmaceutical, or clinical research settings
- Experience with project management tools used commonly in the life sciences industry.
- Experience with detailed, analytical timeline tracking and planning.
- Strong organizational and project management skills
- Ability to manage competing priorities and other tasks as needed
- PMP or similar certification (a plus, not required)
- Experience with financial planning cycles
- Small to mid-size Biotech company experience
- Strong execution and organizational skills
- Ability to manage multiple priorities in a fast-paced environment
- Effective cross-functional communication and collaboration
- Attention to detail with the ability to see the bigger picture
- Proactive, solutions-oriented mindset
- 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.
Base Salary: $130,000 - $180,000. Exact compensation may vary based on level, skills and experience
Salary : $130,000 - $180,000