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HomeCompaniesArtivabioManager / Senior Manager, Clinical Project Management

Manager / Senior Manager, Clinical Project Management

Artivabio · San Diego, California, 92121, United States · Active · BambooHR

Job facts

FieldValue
CompanyArtivabio
TitleManager / Senior Manager, Clinical Project Management
Normalized title-
Department / team-
LocationSan Diego, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-05-07 / 2026-05-30
Changed / last seen2026-05-30 / 2026-07-22

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Company jobsActive postings from Artivabio.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in San Diego.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyArtivabio
Sourcead291a59-704c-402c-bc93-8124ad2a8b38
ATS providerBambooHR

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 : 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 Risk & Issue Management 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. Data Tracking & Reporting 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 Governance & Communication 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 Preferred PMP or similar certification (a plus, not required) Experience with financial planning cycles Small to mid-size Biotech company experience Core Competencies 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 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 - $180,000. Exact compensation may vary based on level, skills and experience

Full job record

Job IDb9481eae745b79bc7fac5e07aff16e45d8ce4482
Org ID71201002-1845-4ebc-99ae-741a04b77221
Source IDad291a59-704c-402c-bc93-8124ad2a8b38
Board IDad291a59-704c-402c-bc93-8124ad2a8b38
Providerbamboohr
Provider Job Key189
TitleManager / Senior Manager, Clinical Project Management
Normalized Title
Statusactive
Activeyes
Location TextSan Diego, California, 92121, United States
Department
Team
Employment Typefull_time
Workplace Type
Remote Policy
CountryUnited States
Region
CitySan Diego
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://artivabio.bamboohr.com/careers/189
Apply URLhttps://artivabio.bamboohr.com/careers/189
First Seen At2026-05-30 06:03:16Z
Last Seen At2026-07-22 10:46:26Z
Last Checked At2026-07-22 10:46:26Z
Last Changed At2026-05-30 06:03:16Z
Inactive At
Source Posted At2026-05-07 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=artivabio/date=2026-07-22/2026-07-22T10-46-24-663Z-ecb6de68033eb409dcef2ddf0a611445feb9d11edbd06bf55d4cfe38233ac083.json
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    "description": "<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt; font-weight: bold\">About Artiva:</span></p>\n<p><span style=\"color: rgb(6, 30, 42)\">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,<span> </span></span><a href=\"https://www.artivabio.com/nk-cell-technology/#topic-1\" target=\"_blank\" rel=\"noopener noreferrer\">AlloNK®</a><span style=\"color: rgb(6, 30, 42)\">, 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.</span></p>\n<p><br></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">For more information, visit <a href=\"https://www.artivabio.com/\" target=\"_blank\" rel=\"noopener noreferrer\">www.artivabio.com</a>.</span></p>\n<p><br></p>\n<p><span style=\"font-size: 12pt\"><span style=\"font-weight: bold\">Job Summary</span>:</span></p>\n<p><span style=\"font-size: 12pt\">We are seeking a Clinical Project Manager to drive cross-functional planning, tracking, and operational integration across clinical-stage programs.</span></p>\n<p><span style=\"font-size: 12pt\"> </span></p>\n<p><span style=\"font-size: 12pt\">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.</span></p>\n<p><span style=\"font-size: 12pt\"> </span></p>\n<p><span style=\"font-size: 12pt\">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</span></p>\n<p><br><br></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Duties/Responsibilities:</span></p>\n<p><span style=\"font-size: 12pt\"> </span></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Timeline Tracking and Integration</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Responsible for creating, maintaining and communicating cross-functional development project management plans at the task, study and molecule levels</span></li>\n<li><span style=\"font-size: 12pt\">Responsible for producing cross functional Project Management tools/visuals/GANTS as required in support of the development team in industry standard software packages</span></li>\n<li><span style=\"font-size: 12pt\">Communicating changes, impacts and potential mitigations across the development team and working to align the cross functional team on best path forward</span></li>\n<li><span style=\"font-size: 12pt\">Support to the finance organization regarding timeline models, changes, and Financial Planning and Analysis integration.</span></li>\n<li><span style=\"font-size: 12pt\">Support communication across internal teams and external stakeholders</span></li>\n</ul>\n<p><span style=\"font-size: 12pt\"> </span></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Risk &amp; Issue Management</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Identify, assess, and track cross-functional risks and dependencies across the development team space.</span></li>\n<li><span style=\"font-size: 12pt\">Communicate to higher organizational structures status, timeline changes and impacts to cross functional deliverables to support mitigation planning.</span></li>\n<li><span style=\"font-size: 12pt\">Develop and maintain the cross-functional risk register for the development team.</span></li>\n<li><span style=\"font-size: 12pt\">Ensure timely tracking and modeling of the impact of critical risks impacting program timelines, quality, or strategic milestones</span></li>\n</ul>\n<ul>\n<li><span style=\"font-size: 12pt\">Support leadership governance activities through preparation of timeline models and scenarios in support of risk assessments. materials.</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Data Tracking &amp; Reporting</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Develop and maintain dashboards to support development team in data tracking and communication to Senior Management</span></li>\n<li><span style=\"font-size: 12pt\">Prepare clear, concise program updates for cross-functional teams and leadership</span></li>\n<li><span style=\"font-size: 12pt\">Ensure consistent reporting across ongoing clinical studies</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Governance &amp; Communication</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Support cross-functional governance meetings, including agenda setting, materials preparation, decision tracking, and follow-up actions</span></li>\n<li><span style=\"font-size: 12pt\">Ensure decisions, actions, and dependencies are clearly documented and tracked</span></li>\n<li><span style=\"font-size: 12pt\">Drive accountability across teams for agreed-upon deliverablesRequirements:</span></li>\n</ul>\n<ul>\n<li><span style=\"font-size: 12pt\">Bachelor’s degree in life sciences or related field</span></li>\n<li><span style=\"font-size: 12pt\">5–8+ years of experience of program management in biotechnology, pharmaceutical, or clinical research settings</span></li>\n<li><span style=\"font-size: 12pt\">Experience with project management tools used commonly in the life sciences industry.</span></li>\n<li><span style=\"font-size: 12pt\">Experience with detailed, analytical timeline tracking and planning.</span></li>\n<li><span style=\"font-size: 12pt\">Strong organizational and project management skills</span></li>\n<li><span style=\"font-size: 12pt\">Ability to manage competing priorities and other tasks as needed</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Preferred</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">PMP or similar certification (a plus, not required)</span></li>\n<li><span style=\"font-size: 12pt\">Experience with financial planning cycles</span></li>\n<li><span style=\"font-size: 12pt\">Small to mid-size Biotech company experience</span></li>\n<li>\n</li></ul>\n<p><span style=\"font-size: 12pt; font-weight: bold\">Core Competencies</span></p>\n<ul>\n<li><span style=\"font-size: 12pt\">Strong execution and organizational skills</span></li>\n<li><span style=\"font-size: 12pt\">Ability to manage multiple priorities in a fast-paced environment</span></li>\n<li><span style=\"font-size: 12pt\">Effective cross-functional communication and collaboration</span></li>\n<li><span style=\"font-size: 12pt\">Attention to detail with the ability to see the bigger picture</span></li>\n<li><span style=\"font-size: 12pt\">Proactive, solutions-oriented mindset</span></li>\n</ul>\n<p><span style=\"font-size: 12pt\"> </span></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">In addition to a great culture, we offer:</span></p>\n<ul>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">A beautiful facility </span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">An entrepreneurial, highly collaborative, and innovative environment</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Comprehensive benefits, including:</span></li>\n</ul>\n<ul>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Medical, Dental, and Vision</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Group Life Insurance</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Long Term Disability (LTD)</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">401(k) Retirement Plan</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Employee Assistance Program (EAP)</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Flexible Spending Account (FSA)</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Paid Time Off (PTO)</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Company paid holidays, including the year-end holiday week</span></li>\n<li><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.</span></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">If all this speaks to you, come join us on our journey!</span></p>\n<p><br></p>\n<p><span style=\"font-family: arial, helvetica, sans-serif; font-size: 12pt\">Base Salary: $130,000 - $180,000. 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