Senior Clinical Research Associate (Healthcare, 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 contribute to the success of clinical trials by ensuring data integrity and participant safety throughout the study lifecycle.

Qualifications

• Advanced degree in life sciences, nursing, or medicine.
• 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 with strong organizational and problem-solving skills.

Responsibilities

• Monitor clinical trial sites for adherence to study protocols and Good Clinical Practice (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 compliance within a complex environment.

Education

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.

Tools

• Relevant clinical trial software and tools.