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

📋 Description

• Design and evaluate clinical trials while interpreting intricate medical data.

• Participate in clinical trial monitoring activities and take ownership of deliverables.

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

• Ensure compliance with protocols, maintain data integrity, and prioritize patient safety throughout the trial process.

• Collaborate with investigators and site personnel to ensure the smooth execution of studies.

• Perform data reviews and resolve queries to uphold high-quality clinical data.

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

• Focus on early-stage development clinical trials (non-oncology).

⛳️ Requirements

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

• A minimum of 2 years of experience as a Clinical Research Associate.

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

• At least 2 years of Phase I experience as a CRA within any therapeutic area.

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

• Capability to work both independently and collaboratively in a fast-paced setting.

• Willingness to travel as necessary (approximately 65-75%) in the West region.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension schemes.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Opportunities for learning and development through structured training and career pathways.