Senior Clinical Scientist

Jade Biosciences

Senior Clinical Scientist at Jade Biosciences supporting clinical development programs in nephrology. Role focuses on rare or immune-mediated kidney diseases and late-stage clinical trials.

Posted 7/25/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $175,000 - $190,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial design and execution, with a strong focus on protocol development, data quality oversight, and regulatory compliance. Proficient in collaborating with cross-functional teams to ensure successful study outcomes and regulatory submissions.

Highest-signal resume keywords

Clinical Research ExperiencePhase 2 And/Or Phase 3 TrialsICH-GCP KnowledgeProject Management SkillsData Review And Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial DesignProtocol DevelopmentData Management CollaborationSafety Management PlansRegulatory SubmissionsStatistical Analysis PlansInformed Consent FormsClinical Study ReportsStudy ManualsMedical Monitoring

Soft Skills

Communication SkillsOrganizational SkillsIndependent WorkMultitasking Ability

Certifications & Qualifications

Advanced Degree In Life SciencesPharmDPhDMSMPH

Industry Keywords

BiotechnologyPharmaceuticalCRO IndustryFDA RegulationsEMA RegulationsClinical Data ReviewStudy Start-UpEnrollmentTrial ExecutionClose-Out Activities

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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