This is a fully remote position, open to applicants in Florida, +2 more locations.

📋 Description

• Supervise and direct clinical trial operations in alignment with protocols, regulatory mandates, and industry benchmarks.

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

• Evaluate clinical trial sites for compliance with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Perform site visits to assess site efficacy, address challenges, and support the successful execution of trials.

• Collaborate with interdisciplinary teams to ensure timely and precise data gathering and reporting.

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

• Establish and nurture relationships with site staff and stakeholders to ensure seamless trial operations.

⛳️ Requirements

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

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

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

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

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

• Availability to travel as needed (approximately 60%).

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