Oncology Clinical Research Lead — Multi-Site CRA

ICON; Sacramento (CA); Presencial; USD 111.000 - 138.000; Jornada completa

Descripción de la vacante

ICON Senior Clinical Research Associate for Phase I Oncology studies oversees clinical trial activities at multiple sites to ensure protocol adherence, regulatory compliance, and data integrity while mentoring junior staff.

Responsibilities include monitoring, site visits, data reporting, staff training, and building strong relationships with investigators and stakeholders to ensure smooth trial operations. Willingness to travel ~60% is required.

Formación

• Bachelor's degree in relevant scientific or healthcare discipline.
• Extensive CRA experience with strong trial process knowledge.
• Ability to manage multiple sites and projects concurrently.
• Expertise in monitoring, data integrity, and site management.
• Current oncology monitoring experience.
• Willingness to travel ~60%.
• Strong communication and stakeholder management skills.

Responsabilidades

• Monitor trial sites for protocol adherence, regulatory compliance, and GCP.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with cross-functional teams on data collection and reporting.
• Train and guide site staff and other CRAs on trial conduct standards.
• Build and maintain relationships with site personnel and stakeholders.

Conocimientos

Strong communication

Stakeholder management

Site management

Multi-site coordination

Educación

Bachelor's degree in a relevant field

Descripción del empleo

ICON Senior Clinical Research Associate for Phase I Oncology studies oversees clinical trial activities at multiple sites to ensure protocol adherence, regulatory compliance, and data integrity while mentoring junior staff.

Responsibilities include monitoring, site visits, data reporting, staff training, and building strong relationships with investigators and stakeholders to ensure smooth trial operations. Willingness to travel ~60% is required.