Clinical Research Program Lead: Operations & Growth

Weill Cornell Medicine; New York (NY); Presencial; USD 120.000 - 160.000; Jornada completa

Descripción de la vacante

Weill Cornell Medicine in New York, NY seeks a Program Manager to oversee clinical research portfolios across disease areas, ensuring feasibility, timely execution, and alignment with priorities.

The role requires 6+ years in clinical research, supervisory experience, and strong knowledge of FDA, OHRP, and ICH-GCP guidelines. This position emphasizes collaboration across departments and regulatory compliance in a busy academic setting.

Formación

• Bachelor's Degree in related field required.
• Advanced degree may be considered in lieu of experience.
• 6+ years of experience in clinical research setting with exposure to a team research environment at all levels.

Responsabilidades

• Serve as the central point person for disease program-level matters and coordinate across operations, finance, contracts, regulatory, and ancillary teams.
• Provide operational guidance to multiple multi-disciplinary clinical research programs and monitor performance, risks, and timelines.
• Oversee initiation, conduct, and closeout across the portfolio ensuring consistency and efficiency.
• Evaluate feasibility of new studies, guides prioritization and activation strategies to optimize timelines.
• Support growth and development of clinical research within assigned services.
• Facilitate cross-departmental collaborations to enhance research capabilities.
• Assist investigators with development of study documents, grants, and presentations.

Conocimientos

FDA Regulations

OHRP Guidance

ICH GCP

Communication

MS Office

Organization

Analytical Skills

Multitasking

Educación

Bachelor's Degree in related field

Herramientas

MS Office Suite

Database Applications

Descripción del empleo

Weill Cornell Medicine in New York, NY seeks a Program Manager to oversee clinical research portfolios across disease areas, ensuring feasibility, timely execution, and alignment with priorities.

The role requires 6+ years in clinical research, supervisory experience, and strong knowledge of FDA, OHRP, and ICH-GCP guidelines. This position emphasizes collaboration across departments and regulatory compliance in a busy academic setting.