Senior Clinical Scientist

🕒 July 25

🇺🇸 United States – Remote

💵 $175k - $190k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 8%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Jade Biosciences

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2024

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

Healthcare • Manufacturing • Biotechnology

Jade Biosciences is a clinical-stage biotechnology company developing potentially best-in-class therapies aimed at transforming the standard of care for autoimmune diseases. Its lead candidate, JADE101, is an antibody designed to inhibit the cytokine APRIL (A PRoliferation-Inducing Ligand) and is being developed for the treatment of immunoglobulin A nephropathy (IgAN). The company builds its pipeline from discovery-stage assets licensed from Paragon Therapeutics and is focused on advancing clinical programs to deliver new treatments for patients with autoimmune conditions.

📋 Description

• 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. • 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. • Support preparation of regulatory submissions and agency interactions.

🎯 Requirements

• 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.

🏖️ Benefits

• Periodic travel for investigator meetings, study team meetings, conferences, and other business activities