Clinical Research Associate II (Healthcare, Remote)

Job summary

The role involves contributing to clinical trial monitoring activities, ensuring compliance with protocols, and collaborating with site staff to facilitate effective study conduct.

Qualifications

• Bachelor's degree in a scientific or healthcare-related discipline.
• At least 2 years of experience in clinical trial monitoring.
• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills with a keen attention to detail.
• Ability to work both independently and as part of a team in a dynamic environment.
• Willingness to travel approximately 60% of the time.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to ensure smooth study execution.
• Perform data review and resolve queries to maintain high-quality clinical data.
• Assist in the preparation and review of study documentation, including protocols and clinical study reports.

Skills

• In-depth knowledge of clinical trial processes and regulations.
• Strong organizational and communication skills.
• Attention to detail and ability to work in a fast-paced environment.

Education

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

Tools

• Familiarity with clinical trial management systems and data management tools.