Clinical Research Associate

This is a fully remote position, open to applicants in New Zealand.

📋 Description

• Execute site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Guarantee adherence to protocols, data integrity, and patient safety throughout the trial lifecycle.

• Collaborate with investigators and site personnel to ensure seamless study implementation.

• Conduct data review and resolve queries to uphold the quality of clinical data.

• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.

• Assume responsibility for clinical trial monitoring deliverables and foster collaborative efforts.

⛳️ Requirements

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

• At least 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a strong attention to detail.

• Capability to work independently and as part of a team in a dynamic environment.

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

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Learning and development prospects through structured training and career pathways.