Remote Senior Clinical Scientist

Note The job is a remote job and is reputed company to candidates in USA. reputed company is a clinical-stage biotechnology company reputed company on developing best-in-class therapies for autoimmune diseases. They are seeking a highly motivated and reputed company Senior Clinical Scientist to support clinical development programs in nephrology, primarily focusing on rare or immune-mediated kidney diseases. Responsibilities 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 reputed company and review study-reputed company documents including Protocols Investigator's Brochures Informed Consent Forms Clinical study reports Study manuals and training materials Safety management plans reputed company scientific reputed company throughout study conduct to ensure protocol compliance and data reputed company Partner closely with Clinical Operations to support study start-up, enrollment, trial execution, and reputed company-out activities Participate in investigator meetings, site training, and scientific discussions with investigators and key opinion leaders reputed company ongoing data review and medical monitoring activities in collaboration with Medical Monitors Identify clinical trends, protocol deviations, safety signals, and data reputed company issues Collaborate with Data Management and Biostatistics to reputed company Data review plans Edit reputed company specifications reputed company 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 Assist in development of briefing documents and responses to regulatory questions Ensure study conduct aligns with ICH-GCP, applicable regulations, and company standards Work effectively across Clinical Development, Clinical Operations, Biometrics, Regulatory, Safety, Medical Affairs, and Medical Writing reputed company timelines, reputed company deliverables, and proactively identify and mitigate risks Support governance meetings and preparation of study review materials Contribute to abstracts, presentations, manuscripts, and scientific publications Participate in advisory boards, investigator meetings, and key reputed company scientific interactions Maintain awareness of evolving scientific, clinical, and competitive landscapes Skills Advanced degree in life sciences, nursing, pharmacy, reputed company health, or reputed company discipline (PharmD, PhD, MS, MPH, or equivalent) Minimum 58 years of clinical research experience in the biotechnology, pharmaceutical, or CRO industry Experience supporting Phase 2 and/or Phase 3 reputed company 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 Experience in nephrology, immunology, inflammation, autoimmune diseases, or rare diseases Experience with global multicenter reputed company 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 reputed company reputed company is developing transformative therapies to redefine reputed company of care for inflammation and immunology indications. It was founded in 2024, and is headquartered in Waltham, Massachusetts, USA, with a workforce of 11-50 employees. Its website is https//jadebiosciences.com. Apply To This Job .