Job Details

ID #53780324
Estado South Carolina
Ciudad Southsanfrancisco
Tipo de trabajo Full-time
Salario USD TBD TBD
Fuente Zai Lab (US) LLC
Showed 2025-04-09
Fecha 2025-04-09
Fecha tope 2025-06-08
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Executive Director, Clinical Science

South Carolina, Southsanfrancisco 00000 Southsanfrancisco USA
Aplica ya

Reporting to the SVP, Global Clinical Development, the Executive Director Clinical Science drives the scientific rigor and integrity of our clinical research programs. This role involves the development of clinical protocols to ensure clinical trials meet regulatory standards and include unbiased and well-controlled clinical design. The Executive Director will collaborate closely with cross-functional teams, including clinical operations, translational medicine, regulatory affairs, and medical affairs, to ensure the seamless execution of clinical trials that meet the highest standards of quality and compliance. The position will be based in our office in South San Francisco, CA.Develop and implement standards for clinical protocols, including data monitoring and preparation of clinical data to ensure consistency and quality.Lead strategic collaborations with colleagues across various departments to gather input and refine clinical protocols.Work closely with study physicians to analyze and interpret clinical trial data, ensuring accuracy and integrity in data reporting.Lead the creation, review, and submission of key clinical documents such as protocols, informed consent forms, clinical study reports, and regulatory submissions.Collaborate with regulatory affairs to support regulatory strategy development, submissions and interactions with health authorities.Work closely with other departments within R&D to align clinical science activities with broader company objectives, including business development diligence.Build and manage a team of clinical science professionals, fostering a culture of excellence and continuous learning.Engage with key stakeholders, including clinical investigators, key opinion leaders, patient advocacy groups, and academic institutions, to advance clinical research initiatives.Ensure compliance with all applicable regulatory standards and ethical guidelines in the conduct of clinical research.Work across several time zones and travel up to 30%.

Aplica ya Suscribir Reportar trabajo