This is a fully remote position, open to applicants in California.

📋 Description

• Oversee and direct clinical trial operations in alignment with protocols, regulatory standards, and industry best practices.

• Lead clinical trial monitoring responsibilities that require technical expertise, emphasizing quality and continuous enhancement.

• Supervise clinical trial sites to ensure compliance with study protocols, regulatory demands, and Good Clinical Practice (GCP) standards.

• Conduct site visits to evaluate site performance, address challenges, and support effective trial execution.

• Collaborate with cross-functional teams to guarantee timely and precise data collection and reporting.

• Offer training and support to site staff and other Clinical Research Associates (CRAs).

• Establish and nurture relationships with site personnel and stakeholders to facilitate seamless trial operations.

⛳️ Requirements

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

• Significant experience as a Clinical Research Associate, with a comprehensive understanding of clinical trial processes and regulatory requirements.

• Demonstrated capability to manage multiple sites and projects concurrently, with strong organizational and problem-solving skills.

• Proficiency in monitoring practices, data integrity, and site management, as well as familiarity with relevant clinical trial software and tools.

• Outstanding communication, interpersonal, and stakeholder management skills, with the capacity to influence and ensure compliance within a complex environment.

• Willingness to travel as necessary (approximately 60%).

• Current experience in Oncology monitoring.

• Legal authorization to work in the country where the position is based.