[All remote jobs](https://jobicy.com/jobs.md)[![Jade Biosciences logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2026/11/07b1366a60be-221.webp)](https://jobicy.com/company/jade-biosciences.md)[Jade Biosciences](https://jobicy.com/company/jade-biosciences.md) # Sr./Clinical Trial Manager AI Summary Jade Biosciences is seeking a Senior Clinical Trial Manager to support planning and operational execution of clinical studies across early- and late-stage development. The role manages trial plans, vendors, CROs, budgets, timelines, risks, documentation, and operational performance across global studies. It requires strong knowledge of GCP, FDA and ICH requirements, Trial Master File standards, and clinical site oversight. The successful candidate will coordinate cross-functional teams and mentors junior Clinical Operations colleagues while escalating material issues with clear recommendations. This remote role includes periodic travel to team and company events.[Apply for this job](#job-application)[View company](https://jobicy.com/company/jade-biosciences.md)ShareRemote from[USA](https://jobicy.com/job-region/usa.md), [Canada](https://jobicy.com/job-region/canada.md)SalaryUSD 180k–195k / yrDepartment[Project & Program Management](https://jobicy.com/categories/project-management.md)EmploymentFull TimeExperienceDirectorPublished12 Nov 2026Apply before12 Dec 2026Listing views46Application actions3Application toolkit ## Make your next move. Prepare your resume, explore your fit, and draft a cover letter for this opportunity. Opportunity details ## About this role. About [Jade Biosciences](https://jobicy.com/company/jade-biosciences.md) 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 [JadeBiosciences.com](https://url.usb.m.mimecastprotect.com/s/kwQpCrgGLMHxLkBujt66i4Vdxs?domain=globenewswire.com) and follow the Company on [LinkedIn](https://url.usb.m.mimecastprotect.com/s/S9DbCvmMP9TvMYkC5ulliQtFaR?domain=globenewswire.com). Role Overview The Sr/Clinical Trial Manager will support the Director, Clinical Operations, who is the cross functional clinical trial leader, in the planning and operational execution of assigned clinical trials. This individual will coordinate day-to-day study activities across cross-functional partners, clinical sites, CROs, and other vendors; maintain study plans, timelines, budgets, risks, and key documentation; and escalate issues with clear recommendations. The Senior/Clinical Trial Manager will serve as a primary operational contact for assigned responsibilities, vendors, and regions and help ensure trials are delivered on time, within budget, and in compliance with applicable regulations, Good Clinical Practice, and company standards.  With a proven track record of clinical trial management, financial acumen, and problem-solving skills, this individual will thrive in Jade’s dynamic environment. This is an exciting opportunity to make significant contributions to Jade’s immunology pipeline, managing trials from first in human single site to global (APAC, LATAM, etc.) phase 3. Key Responsibilities * 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  * 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  * Maintain clinical trial budgets and forecasts; review invoices, track committed and actual spend, identify variances, and escalate financial risks to the Director  * Maintain study risk, issue, decision, and action logs; drives mitigation and resolution activities and promptly escalates material risks with recommended options  * 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  * Oversee global or regional study start-up, site activation, enrollment, conduct, monitoring, closeout, and inspection-readiness activities for assigned trials  * Support planning and conducting investigator meetings in alignment with Director guidance * 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. * Build effective working relationships with clinical sites, investigators, CROs, vendors, and internal stakeholders and serves as a key operational point of contact  * 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  * Ensure clinical trial activities and documentation comply with the protocol, Good Clinical Practice, applicable regulations, contractual requirements, and company procedures  * Support clinical supply, central laboratory, data management, safety, biostatistics, medical monitoring, and regulatory activities by coordinating operational requirements and timelines  * Oversee the maintenance of a complete, accurate, and inspection-ready Trial Master File documentation and supports audits, inspections, and quality oversight activities  * Mentor Clinical Trial Associates and Clinical Trial Managers; contributes to Clinical Operations process improvements, and prepare clear study updates for governance and senior leadership  Qualifications * Bachelors and10+ years of related experience for Sr Clinical Trial Manager and 7+ years of related experience for the Clinical Trial Manager * 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  * Experience supporting Phase 1 through Phase 3 clinical trials; global clinical trial experience is preferred  * Immunology and/or rare disease clinical trial experience is preferred  * Experience managing CROs and clinical vendors, including laboratories, RTSM, EDC, and ancillary clinical technology or applications  * Strong working knowledge of FDA regulations, ICH guidelines, Good Clinical Practice, medical terminology, and clinical trial conduct  * Working knowledge of clinical protocol implementation, regulatory submissions, Trial Master File requirements, and the overall drug development process  * Experience mentoring or providing day-to-day guidance to junior team members is preferred  * Excellent communication, organization, collaboration, problem-solving, and attention-to-detail skills, with the ability to manage competing priorities  Position Location This is a remote role; periodic travel to team and company events is required. The anticipated salary range for candidates for the Sr Clinical Trial Manager: $180,000 – 195,000, Clinical Trial Manger: $155,000 – $175,000. The final salary offered will depend on several factors, which may include, but not limited to, relevant years of experience, educational background, and geography. 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 [poster](https://www.e-verify.gov/sites/default/files/everify/images/manuals/EVParticipationPoster.JPG). 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. Show more [Apply now >](https://jobicy.com/jobs/161705-sr-clinical-trial-manager.md) * ![Upload CV](data:image/svg+xml;base64,PHN2ZyB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciIHdpZHRoPSI2NSIgaGVpZ2h0PSI2NSIgZmlsbD0ibm9uZSIgeG1sbnM6dj0iaHR0cHM6Ly92ZWN0YS5pby9uYW5vIj48ZyBjbGlwLXBhdGg9InVybCgjQSkiPjxwYXRoIGQ9Ik0wIDBINjVWNjVIMFYwWiIgZmlsbD0iIzAyOWFlYiIvPjxnIGZpbGw9IiNmZmYiIHN0cm9rZT0iI2ZmZiIgc3Ryb2tlLXdpZHRoPSIyIj48cGF0aCBkPSJNMzMuMDQ5IDE1LjQ1NGExLjQzIDEuNDMgMCAwIDAtMi4wOTcgMGwtNy41NzkgOC4xNDdhMS4zOCAxLjM4IDAgMCAwIC4wOSAxLjk3MyAxLjQ0IDEuNDQgMCAwIDAgMi4wMDgtLjA4OGw1LjEwOS01LjQ5MnYyMC42MWExLjQxIDEuNDEgMCAwIDAgMS40MjEgMS4zOTdjLjc4NSAwIDEuNDIxLS42MjUgMS40MjEtMS4zOTd2LTIwLjYxbDUuMTA5IDUuNDkyYTEuNDQgMS40NCAwIDAgMCAyLjAwOC4wODggMS4zOCAxLjM4IDAgMCAwIC4wOS0xLjk3M2wtNy41NzktOC4xNDZ6TTE2Ljc2OSAzOC40YzAtLjc3My0uNjItMS40LTEuMzg1LTEuNFMxNCAzNy42MjcgMTQgMzguNHYuMTAybC4yMTUgNi4yMjljLjIyMyAxLjY4LjcwMSAzLjA5NSAxLjgxMyA0LjIxOHMyLjUxIDEuNjA3IDQuMTcyIDEuODMzYzEuNi4yMTggMy42MzYuMjE4IDYuMTYuMjE4aDExLjI4bDYuMTYtLjIxOGMxLjY2Mi0uMjI2IDMuMDYxLS43MDkgNC4xNzItMS44MzNzMS41ODktMi41MzggMS44MTMtNC4yMThDNTAgNDMuMTEzIDUwIDQxLjA1NSA1MCAzOC41MDNWMzguNGMwLS43NzMtLjYyLTEuNC0xLjM4NS0xLjRzLTEuMzg1LjYyNy0xLjM4NSAxLjRsLS4xOSA1Ljk1OGMtLjE4MiAxLjM3LS41MTUgMi4wOTUtMS4wMjYgMi42MTJzLTEuMjI4Ljg1My0yLjU4MyAxLjAzOGMtMS4zOTUuMTktMy4yNDMuMTkzLTUuODkzLjE5M0gyNi40NjJjLTIuNjUgMC00LjQ5OC0uMDAzLTUuODkzLS4xOTMtMS4zNTUtLjE4NC0yLjA3Mi0uNTIxLTIuNTgzLTEuMDM4cy0uODQ0LTEuMjQyLTEuMDI2LTIuNjEyYy0uMTg3LTEuNDEtLjE5MS0zLjI3OS0uMTkxLTUuOTU4eiIvPjwvZz48L2c+PGRlZnM+PGNsaXBQYXRoIGlkPSJBIj48cGF0aCBmaWxsPSIjZmZmIiBkPSJNMCAwaDY1djY1SDB6Ii8+PC9jbGlwUGF0aD48L2RlZnM+PC9zdmc+) ### Upload your resume now To unlock remote work opportunities and be discovered by global employers. This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content. ## Role DNA A quick view of the complexity, pace, ownership and collaboration implied by the job description. ### Job Complexity 5/5EasyHard ### Pace & Pressure 5/5RelaxedFast-paced ### Autonomy Level 4/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThis is a senior clinical operations role requiring more than 10 years of relevant experience and accountability for complex, global Phase 1 through Phase 3 trials. The position combines regulatory compliance, vendor leadership, financial oversight, risk management, and cross-functional coordination in a fast-moving biotech environment. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$187,500US market range (per year)$170k–$220k0$242.00k AI insightThe yearly pay period is inferred from the job context; it was not explicitly stated by the employer. The employer discloses a base salary range of $180,000 to $195,000 USD for the Senior Clinical Trial Manager role. The posting does not explicitly state a pay cadence, so yearly compensation is inferred from the compensation level, seniority, and US biotechnology market context. A reasonable estimated US market range for a senior clinical trial management role is $170,000 to $220,000 USD per year. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical trial management](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20management.md)[Clinical operations](https://jobicy.com/jobs?search_keywords=Clinical%20operations.md)[Good Clinical Practice](https://jobicy.com/jobs?search_keywords=Good%20Clinical%20Practice.md)[ICH guidelines](https://jobicy.com/jobs?search_keywords=ICH%20guidelines.md)[FDA regulations](https://jobicy.com/jobs?search_keywords=FDA%20regulations.md)[CRO management](https://jobicy.com/jobs?search_keywords=CRO%20management.md)[Vendor oversight](https://jobicy.com/jobs?search_keywords=Vendor%20oversight.md)[Clinical trial budgeting](https://jobicy.com/jobs?search_keywords=Clinical%20trial%20budgeting.md)[Risk management](https://jobicy.com/jobs?search_keywords=Risk%20management.md)[Trial Master File](https://jobicy.com/jobs?search_keywords=Trial%20Master%20File.md)[Study start-up](https://jobicy.com/jobs?search_keywords=Study%20start-up.md)[Site activation](https://jobicy.com/jobs?search_keywords=Site%20activation.md)[Clinical monitoring](https://jobicy.com/jobs?search_keywords=Clinical%20monitoring.md)[Cross-functional collaboration](https://jobicy.com/jobs?search_keywords=Cross-functional%20collaboration.md)[Inspection readiness](https://jobicy.com/jobs?search_keywords=Inspection%20readiness.md) Sample interview questionsDescribe your experience overseeing a clinical trial from study start-up through closeout.I establish an integrated operational plan covering timelines, country and site activation, vendor deliverables, enrollment assumptions, monitoring, data review, budget tracking, and TMF readiness. I use routine governance reviews and risk logs to identify gaps early, align owners on corrective actions, and maintain inspection readiness through closeout. How do you manage CRO and vendor performance during a study? I set clear scopes of work, deliverables, KPIs, governance cadences, and escalation pathways at the outset. I review performance data, invoices, monitoring outputs, and issue trends regularly, document decisions, and work with vendors on corrective and preventive actions when performance deviates from expectations. What approach would you take when enrollment is behind forecast? I would first validate the underlying data and determine whether the barrier is site activation, patient identification, competition, protocol burden, or site performance. I would then propose targeted actions such as activating additional sites, improving site engagement, revising recruitment tactics where permitted, and updating forecasts and risks for leadership review. How do you ensure clinical trial activities remain compliant with GCP and applicable regulations? I build compliance into operational plans, vendor oversight, monitoring expectations, document review, and TMF quality controls. I routinely review monitoring reports and metrics, address deviations and trends promptly, confirm that required documentation is complete, and escalate significant compliance risks with recommended actions. How have you managed competing priorities across multiple clinical stakeholders? I use a transparent plan with clear milestones, decision logs, accountable owners, and regular cross-functional updates. I prioritize work based on patient safety, regulatory obligations, critical path impact, and financial risk, while escalating trade-offs early so that decisions are timely and well documented. Next step ## Apply now. Follow the employer’s application method and review Jobicy’s safety guidance before sharing personal information. 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