Clinical Trial Start-Up Lead: Site Activation & Submissions

ICON Clinical Research; España; A distancia; EUR 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life assurance

Descripción de la vacante

ICON Strategic Solutions is seeking a Principal, Study Start Up Associate to lead clinical trial start-up activities. You will coordinate site activation, ensure regulatory compliance, and collaborate with project management, clinical operations, and regulatory affairs to streamline processes.

The role requires solid start-up experience, strong organizational skills, and the ability to travel about 15% to support sites globally.

Formación

• Solid site start-up and activation experience.
• Ability to manage multiple projects and priorities in a fast-paced environment.
• Excellent organizational skills and attention to detail.
• Willingness to travel approximately 15%.

Responsabilidades

• Leading the preparation and submission of essential documents for regulatory approvals and site activation.
• Collaborating with cross-functional teams, including project management, clinical operations, and regulatory affairs, to streamline study start-up processes.
• Overseeing the identification and selection of clinical sites, ensuring they meet project criteria and compliance standards.
• Providing guidance and support to study teams and sites during the start-up phase, fostering effective communication and collaboration.
• Staying current with industry regulations and trends to enhance start-up strategies and best practices.

Conocimientos

Site start-up experience

Project coordination

Regulatory knowledge

Communication skills

Educación

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Descripción del empleo

ICON Strategic Solutions is seeking a Principal, Study Start Up Associate to lead clinical trial start-up activities. You will coordinate site activation, ensure regulatory compliance, and collaborate with project management, clinical operations, and regulatory affairs to streamline processes.

The role requires solid start-up experience, strong organizational skills, and the ability to travel about 15% to support sites globally.