Medical Director

Key Responsibilities The Medical Director will provide strategic medical leadership across the clinical development lifecycle, driving the design, execution, and interpretation of clinical programs to support the company’s pipeline and regulatory objectives, while building and maintaining strong relationships with clinical investigators and key opinion leaders. Responsibilities • Serve as the lead medical expert and primary authority for assigned clinical programs, with overall responsibility for patient safety oversight and key medical decision-making • Lead the review, analysis, and interpretation of clinical and safety data, translating findings into strategic insights to guide development decisions • Drive the design of clinical trials, including authorship and review of key documents (protocols, IBs, CSRs, and regulatory submissions) • Provide medical leadership across cross-functional teams (e.g. Clinical Operations, Pharmacovigilance, Data Management etc.), ensuring alignment and scientific rigor • Build and maintain strong relationships with clinical investigators and KOLs; lead scientific forums such as Steering Committees and Advisory Boards • Represent the company in interactions with external stakeholders, including regulatory authorities and potential partners, supporting due diligence and business development activities • Lead the development of clinical publications, including abstracts, manuscripts, and presentations in line with publication strategy • Represent the company at investigator meetings, site visits, and international congresses • Lead internal and external training initiatives related to clinical programs and scientific data • Perform additional duties as assigned by the direct manager