[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) # Senior Clinical Scientist AI Summary Jade Biosciences is hiring a Senior Clinical Scientist to support Phase 2 and Phase 3 clinical development programs in nephrology and immune-mediated kidney diseases. The role leads scientific and operational execution activities, including protocol development, data review, medical monitoring, study documentation, and regulatory support. The successful candidate will work cross-functionally with Clinical Operations, Biometrics, Regulatory, Safety, Medical Affairs, and Medical Writing. This fully remote role requires periodic travel for investigator meetings, study team meetings, conferences, and other business activities. Candidates need an advanced life-sciences-related degree and at least 5–8 years of relevant biotech, pharmaceutical, or CRO clinical research experience.[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)SalaryUSD 175k–190k / yrDepartment[Healthcare & Medical](https://jobicy.com/categories/healthcare.md)EmploymentFull TimeExperienceDirectorPublished12 Nov 2026Apply before12 Dec 2026Listing views59Application actions1Application 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 We are seeking a highly motivated and experienced Senior Clinical Scientist to support clinical development programs in nephrology, with a focus on rare or immune-mediated kidney diseases. This individual will play a key role in translating clinical strategy into high-quality execution of late-stage phase clinical trials. This is an exciting opportunity to join a growing biotechnology company where individual contributions have significant impact. The ideal candidate thrives in a fast-paced, collaborative environment, demonstrates strong scientific and operational expertise, and takes ownership of key deliverables. This newly created position will report to the Executive Medical Director of Clinical Development. The role is fully remote and will require periodic travel for investigator meetings, study team meetings, conferences, and other business activities. Key Responsibilities Clinical Development and Study Execution * Serve as the Clinical Scientist for one or more Phase 2 and/or Phase 3 clinical studies. * Contribute to study design, protocol development, and protocol amendments. * Develop and review study-related documents including: * Protocols * Investigator’s Brochures * Informed Consent Forms * Clinical study reports * Study manuals and training materials * Safety management plans * Provide scientific oversight throughout study conduct to ensure protocol compliance and data quality. * Partner closely with Clinical Operations to support study start-up, enrollment, trial execution, and close-out activities. * Participate in investigator meetings, site training, and scientific discussions with investigators and key opinion leaders. Data Review and Interpretation * Lead ongoing data review and medical monitoring activities in collaboration with Medical Monitors. * Identify clinical trends, protocol deviations, safety signals, and data quality issues. * Collaborate with Data Management and Biostatistics to develop: * Data review plans * Edit check specifications * Endpoint derivation and analysis plans * Participate in database lock, data cleaning, and analysis activities. * Contribute to interpretation of study results and development of key messages. Regulatory and Documentation Support * Support preparation of regulatory submissions and agency interactions. * Assist in development of briefing documents and responses to regulatory questions. * Ensure study conduct aligns with ICH-GCP, applicable regulations, and company standards. Cross-Functional Collaboration * Work effectively across Clinical Development, Clinical Operations, Biometrics, Regulatory, Safety, Medical Affairs, and Medical Writing. * Drive timelines, track deliverables, and proactively identify and mitigate risks. * Support governance meetings and preparation of study review materials. Scientific Communication * Contribute to abstracts, presentations, manuscripts, and scientific publications. * Participate in advisory boards, investigator meetings, and key external scientific interactions. * Maintain awareness of evolving scientific, clinical, and competitive landscapes. Qualifications Required * Advanced degree in life sciences, nursing, pharmacy, public health, or related discipline (PharmD, PhD, MS, MPH, or equivalent). * Minimum 5–8 years of clinical research experience in the biotechnology, pharmaceutical, or CRO industry. * Experience supporting Phase 2 and/or Phase 3 clinical trials. * Strong understanding of clinical trial design, clinical data review, and drug development. * Working knowledge of ICH-GCP, FDA, EMA, and global regulatory requirements. * Experience reviewing clinical data and collaborating with biostatistics and data management teams. * Excellent project management, communication, and organizational skills. * Ability to work independently and manage multiple priorities in a fast-paced environment. Preferred * Experience in nephrology, immunology, inflammation, autoimmune diseases, or rare diseases. * Experience with global multicenter clinical trials. * Prior involvement in regulatory submissions and health authority interactions. * Experience contributing to scientific publications and conference presentations. * Experience working in a small or emerging biotechnology company. Skills and Competencies * Strong scientific and analytical thinking * Attention to detail with a focus on data quality * Excellent written and verbal communication skills * Collaborative and team-oriented mindset * Ability to influence across functions without direct authority * Comfortably operating in a highly dynamic, entrepreneurial environment * Proactive, hands-on, and solution-oriented approach Position Location This is a remote role; periodic travel to team and company events is required. The anticipated salary range for candidates for this role is $175,000 – $190,000. 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/161698-senior-clinical-scientist.md) * ![Upload CV](data:image/svg+xml;base64,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) ### 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 5/5GuidedFull ownership ### Communication Load 5/5IndependentCollaborative AI insightThis is a senior clinical development position requiring scientific judgment across late-stage trials, clinical data interpretation, regulatory support, and cross-functional execution. The role demands independent ownership in a fast-moving biotechnology environment while maintaining rigorous ICH-GCP and data-quality standards. ## Salary analysis Estimated compensation compared with the broader US market for similar roles. Estimated job median (per year)Market rate$182,500US market range (per year)$170k–$210k0$231.00k 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 USD 175,000 to USD 190,000. The annual period is inferred from the compensation magnitude, seniority, US biotechnology market, and standard full-time professional compensation conventions because the posting does not explicitly state a cadence. A reasonable estimated US market range for a senior clinical scientist in a clinical-stage biotechnology company is USD 170,000 to USD 210,000 per year. ## Core skills Skills and capabilities most closely associated with this opportunity. [Clinical development](https://jobicy.com/jobs?search_keywords=Clinical%20development.md)[Phase II clinical trials](https://jobicy.com/jobs?search_keywords=Phase%20II%20clinical%20trials.md)[Phase III clinical trials](https://jobicy.com/jobs?search_keywords=Phase%20III%20clinical%20trials.md)[Protocol development](https://jobicy.com/jobs?search_keywords=Protocol%20development.md)[Clinical data review](https://jobicy.com/jobs?search_keywords=Clinical%20data%20review.md)[Medical monitoring](https://jobicy.com/jobs?search_keywords=Medical%20monitoring.md)[ICH-GCP](https://jobicy.com/jobs?search_keywords=ICH-GCP.md)[Regulatory submissions](https://jobicy.com/jobs?search_keywords=Regulatory%20submissions.md)[Clinical study reports](https://jobicy.com/jobs?search_keywords=Clinical%20study%20reports.md)[Data quality management](https://jobicy.com/jobs?search_keywords=Data%20quality%20management.md)[Biostatistics collaboration](https://jobicy.com/jobs?search_keywords=Biostatistics%20collaboration.md)[Clinical operations](https://jobicy.com/jobs?search_keywords=Clinical%20operations.md)[Nephrology](https://jobicy.com/jobs?search_keywords=Nephrology.md)[Scientific communication](https://jobicy.com/jobs?search_keywords=Scientific%20communication.md) Sample interview questionsHow have you contributed to the design and execution of a Phase 2 or Phase 3 clinical trial?I have supported protocol development, study start-up, ongoing scientific oversight, data review, and close-out activities. My approach is to translate clinical objectives into operationally feasible procedures, identify risks early, and partner closely with Clinical Operations, Data Management, and Biostatistics throughout the study lifecycle. What is your approach to reviewing clinical data and identifying potential safety or data-quality issues? I use a structured review plan focused on protocol adherence, patient-level trends, adverse events, laboratory data, endpoints, and missing or inconsistent information. I assess issues in clinical context, escalate meaningful safety signals promptly, and collaborate with medical monitors, data management, and sites to resolve discrepancies. How do you ensure that a clinical study remains compliant with ICH-GCP and applicable regulations? I build compliance into study documents, training, oversight routines, and issue-management processes from the beginning. I stay current on relevant requirements, ensure protocol and informed-consent materials are clear, monitor deviations and corrective actions, and document decisions carefully for inspection readiness. Describe how you manage competing priorities in a fast-paced biotechnology environment. I prioritize work according to patient safety, critical-path timelines, regulatory commitments, and study risks. I maintain transparent deliverable trackers, align frequently with cross-functional stakeholders, raise risks early, and adjust plans quickly when new data or operational constraints emerge. How would you communicate emerging study findings to cross-functional teams and external investigators? I would tailor the level of detail to the audience while keeping the message scientifically accurate, balanced, and evidence-based. For internal teams, I would connect findings to operational and development decisions; for investigators, I would clearly explain the clinical context, protocol implications, and any required actions. Next step ## Apply now. Follow the employer’s application method and review Jobicy’s safety guidance before sharing personal information. Keep exploring ## Related remote jobs. * ![Centria Autism logo](https://jobicy.com/data/server-nyc0409/galaxy/mercury/2025/06/75886de1-221.jpeg) Centria Autism Nov 12 New ### [PM Telehealth Board Certified Behavior Analyst (BCBA)](https://jobicy.com/jobs/161606-pm-telehealth-board-certified-behavior-analyst-bcba.md) Are you a BCBA looking for the flexibility of remote work without giving up clinical impact? 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