Senior Clinical Research Associate (Remote)

Job summary

The role involves overseeing and managing clinical trial activities to ensure compliance with protocols, regulatory requirements, and industry standards. The Senior Clinical Research Associate will lead monitoring tasks with a focus on quality and continuous improvement.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Associate with a strong understanding of clinical trial processes and regulatory requirements
• Proven ability to manage multiple sites and projects simultaneously
• Strong organizational and problem-solving skills

Responsibilities

• Monitor clinical trial sites for adherence to study protocols and GCP standards
• Conduct site visits to assess performance, resolve issues, and support trial execution
• Collaborate with cross-functional teams for timely and accurate data collection and reporting
• Provide training and guidance to site staff and other CRAs
• Build and maintain effective relationships with site personnel and stakeholders

Skills

• Expertise in monitoring practices, data integrity, and site management
• Proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills
• Ability to influence and drive compliance in complex environments

Education

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

Tools

• Relevant clinical trial software and tools