Clinical Research Associate II (Remote)

Job summary

This role involves designing and analyzing clinical trials while interpreting complex medical data to support the advancement of innovative treatments. The position is fully remote and requires collaboration with various stakeholders in the clinical trial process.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%).

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 facilitate smooth study conduct.
• Perform data review and resolve queries to maintain high-quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Skills

• Strong organizational and communication skills.
• Attention to detail.
• Ability to work independently and collaboratively.

Education

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

Tools

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