Sr./Clinical Trial Manager at Jade Biosciences — Remote

About The Role

&lt;div class=&quot;content-intro&quot;&gt;&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;About Jade Biosciences&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559738&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade’s lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated for the treatment of immunoglobulin A nephropathy. Jade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an anti-IFN-β monoclonal antibody. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit&amp;nbsp;&lt;a href=&quot;https://url.usb.m.mimecastprotect.com/s/gdHGCxo0R7SZrNDCWuEEiyeylj?domain=globenewswire.com&quot;&gt;JadeBiosciences.com&lt;/a&gt;&amp;nbsp;and follow the Company on&amp;nbsp;&lt;a href=&quot;https://url.usb.m.mimecastprotect.com/s/yyhPCyp4VJiY9VKtPCmmixqBdf?domain=globenewswire.com&quot;&gt;LinkedIn&lt;/a&gt;.&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Role Overview&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559738&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span class=&quot;TextRun SCXW54446230 BCX0&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;The S&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;r&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;/&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;Clinical Trial Manager will support the Director, Clinical Operations&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;, who is the cross functional clinical trial leader,&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; in the planning and operational execution of assigned clinical trials. This &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;individual&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; will coordinate day-to-day study activities across cross-functional partners, clinical sites, CROs, and other vendors; &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;maintain&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; study plans, timelines, budgets, risks, and key documentation; and escalate issues with clear recommendations. The Senior&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;/&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;Clinical Trial Manager will serve as a primary operational contact for assigned &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;responsibilities&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;, vendors, and regions&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; and help ensure trials are delivered on time, within budget, and in compliance with applicable regulations, Good Clinical Practice, and company standards. &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; With&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; a&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; proven&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;track record&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; of clinical trial management&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;, financial acumen, and problem-solving skills, th&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;is&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; individual &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;will &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;thrive in&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; Jade’s &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;dynamic environment.&lt;/span&gt; &lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;This is an &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;exciting &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;opportunity to make significant contributions to Jade’s immunology pipeline, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;managing&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; trials from first in human single &lt;/span&gt;&lt;span class=&quot;NormalTextRun ContextualSpellingAndGrammarErrorV2Themed SCXW54446230 BCX0&quot;&gt;site&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt; to global (APAC, LATAM, &lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;etc.&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;) phase 3&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;.&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;TextRun MacChromeBold SCXW54446230 BCX0&quot; lang=&quot;EN-US&quot; data-contrast=&quot;none&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW54446230 BCX0&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;EOP Selected SCXW54446230 BCX0&quot; data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Key Responsibilities&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335557856&amp;quot;:16777215,&amp;quot;335559738&amp;quot;:240,&amp;quot;335559739&amp;quot;:240,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support the development, maintenance, and execution on detailed study operational plans, timelines, enrollment projections, and tracking tools in alignment with program strategy and Director guidance &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Responsible for vendor oversight activities, for assigned vendors, including deliverables, performance metrics, issue resolution, meeting governance, invoices, and scope tracking; supports vendor selection and Scope of Work development &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Maintain &amp;nbsp;clinical trial budgets and forecasts; review invoices, track committed and actual spend, identify variances, and escalate financial risks to the Director &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Maintain study risk, issue, decision, and action logs; drives mitigation and resolution activities and promptly escalates material risks with recommended options &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Coordinate operational input into the development, review, and implementation of clinical documents, including protocols, monitoring plans, informed consent forms, investigator brochures, pharmacy and laboratory manuals, and clinical study reports &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Oversee global or regional study start-up, site activation, enrollment, conduct, monitoring, closeout, and inspection-readiness activities for assigned trials &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Support planning and conducting investigator meetings in alignment with Director guidance&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Responsible for monitoring oversight, inclusive of study specific templates and plans, reviewing monitoring reports for compliance to study protocols, regulations and ICF/GCP, tracking and managing monitoring report metrics.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Build effective working relationships with clinical sites, investigators, CROs, vendors, and internal stakeholders and serves as a key operational point of contact &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Review study performance metrics and operational data, identifies trends or gaps, and implements corrective and preventive actions in partnership with the Director and cross-functional team &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Ensure clinical trial activities and documentation comply with the protocol, Good Clinical Practice, applicable regulations, contractual requirements, and company procedures &lt;/span&gt; &lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;Support clinical supply, central laboratory, data management, safety, biostatistics, medical monitoring, and regulatory activities by coordinating operational requirements and timelines &lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Oversee the maintenance of a complete, accurate, and inspection-ready Trial Master File documentation and supports audits, inspections, and quality oversight activities &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Mentor Clinical Trial Associates and Clinical Trial Managers; contributes to Clinical Operations process improvements, and prepare clear study updates for governance and senior leadership &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p style=&quot;line-height: 2;&quot;&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Qualifications&lt;/span&gt;&lt;/strong&gt; &amp;nbsp;&lt;/p&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;1&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Bachelors and10+ years of related experience for Sr Clinical Trial Manager and 7+&amp;nbsp; years of related experience for the Clinical Trial Manager&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;2&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Trial management within a biopharmaceutical company; experience at a small startup is a plus.Demonstrated ability to manage complex clinical trial activities, timelines, vendors, budgets, risks, and cross-functional deliverables with appropriate independence and escalation &lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;335559739&amp;quot;:0}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;3&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience supporting Phase 1 through Phase 3 clinical trials; global clinical trial experience is preferred &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;4&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Immunology and/or rare disease clinical trial experience is preferred &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;5&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience managing CROs and clinical vendors, including laboratories, RTSM, EDC, and ancillary clinical technology or applications &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;6&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Strong working knowledge of FDA regulations, ICH guidelines, Good Clinical Practice, medical terminology, and clinical trial conduct &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;ul&gt;
&lt;li style=&quot;line-height: 2;&quot; data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;7&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Working knowledge of clinical protocol implementation, regulatory submissions, Trial Master File requirements, and the overall drug development process &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot; data-leveltext=&quot;&quot; data-font=&quot;Symbol&quot; data-listid=&quot;15&quot; data-list-defn-props=&quot;{&amp;quot;335552541&amp;quot;:1,&amp;quot;335559685&amp;quot;:720,&amp;quot;335559991&amp;quot;:360,&amp;quot;469769226&amp;quot;:&amp;quot;Symbol&amp;quot;,&amp;quot;469769242&amp;quot;:[8226],&amp;quot;469777803&amp;quot;:&amp;quot;left&amp;quot;,&amp;quot;469777804&amp;quot;:&amp;quot;&amp;quot;,&amp;quot;469777815&amp;quot;:&amp;quot;multilevel&amp;quot;}&quot; data-aria-posinset=&quot;8&quot; data-aria-level=&quot;1&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Experience mentoring or providing day-to-day guidance to junior team members is preferred &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;li style=&quot;line-height: 2;&quot;&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Excellent communication, organization, collaboration, problem-solving, and attention-to-detail skills, with the ability to manage competing priorities &lt;/span&gt;&lt;span data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Position Location&lt;/span&gt;&lt;/strong&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;This is a remote role; periodic travel to team and company events is required.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;The anticipated salary range for candidates for the&lt;/span&gt;&lt;span data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;TextRun SCXW240907745 BCX0&quot; lang=&quot;EN-US&quot; data-contrast=&quot;auto&quot;&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;&amp;nbsp;Sr Clinical Trial Manager&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;:&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt; $1&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;8&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;0,000 – 195,000, Clinical Trial Manger&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;:&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt; amp;amp;lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;1&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;55&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;,000 - $17&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;5&lt;/span&gt;&lt;span class=&quot;NormalTextRun SCXW240907745 BCX0&quot;&gt;,000.&lt;/span&gt;&lt;/span&gt;&lt;span class=&quot;EOP Selected SCXW240907745 BCX0&quot; data-ccp-props=&quot;{}&quot;&gt;&amp;nbsp;The&lt;/span&gt;&amp;nbsp;final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;div class=&quot;content-conclusion&quot;&gt;&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;As part of the I-9 verification of authorization to work in the United States, Jade Bioscience participates in E-Verify. To learn more about E-Verify please review this&amp;nbsp;&lt;/span&gt;&lt;a href=&quot;https://www.e-verify.gov/sites/default/files/everify/images/manuals/EVParticipationPoster.JPG&quot;&gt;&lt;span data-contrast=&quot;none&quot;&gt;&lt;span data-ccp-charstyle=&quot;Hyperlink&quot;&gt;poster&lt;/span&gt;&lt;/span&gt;&lt;/a&gt;&lt;span data-contrast=&quot;auto&quot;&gt;.&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;span data-contrast=&quot;auto&quot;&gt;Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.&lt;/span&gt;&lt;span data-ccp-props=&quot;{&amp;quot;201341983&amp;quot;:0,&amp;quot;335559739&amp;quot;:0,&amp;quot;335559740&amp;quot;:240}&quot;&gt;&amp;nbsp;&lt;/span&gt;&lt;/p&gt;&lt;/div&gt;