Lead the design, execution, and oversight of clinical trials in nephrology. Serve as Medical Monitor for ongoing trials. Collaborate with clinical operations, regulatory, and biometrics teams. Educate and advise clinical sites/investigators. Provide medical expertise and support to external partners, vendors, and contractors. Communicate effectively with internal and external stakeholders. Contribute to the preparation of regulatory documents. Support interactions with regulatory authorities and ethics committees. Stay current with scientific literature and competitive landscape in nephrology. Partner with translational science, biomarker, and commercial teams. Provide medical input into lifecycle planning and early market preparation. Begin building relationships with key opinion leaders (KOLs), investigators, and advocacy groups. Represent the company at scientific meetings, advisory boards, and industry events.