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

📋 Description

• Supervise and direct clinical trial operations in accordance with protocols, regulatory standards, and industry norms.

• Lead monitoring activities for clinical trials that demand technical expertise, emphasizing quality and ongoing enhancement.

• Oversee clinical trial sites to ensure compliance with study protocols, regulatory mandates, and Good Clinical Practice (GCP) guidelines.

• Perform site visits to evaluate site performance, address challenges, and promote effective trial execution.

• Work collaboratively with cross-functional teams to ensure timely and precise data gathering and reporting.

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

• Cultivate and sustain relationships with site staff and stakeholders to ensure seamless trial operations.

⛳️ Requirements

• A Bachelor's degree in a pertinent scientific area or a healthcare-related discipline.

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

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

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

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

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

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