Clinical Research Associate 1

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

📋 Description

• Coordinate all activities involved in the establishment and oversight of clinical studies.

• Prepare precise study status reports and maintain thorough study documentation.

• Efficiently manage sponsor-generated queries and take charge of study cost-effectiveness.

• Engage in the preparation and evaluation of study documentation and feasibility studies for new proposals as needed.

• Foster and sustain collaborative relationships with key stakeholders, clinical investigators, and site personnel.

• Ensure patient safety while adhering to ICON procedures, protocols, and regulatory standards.

⛳️ Requirements

• A university degree in medicine, science, or a related field.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data effectively.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills for timely resolution of inquiries.

• Willingness to travel as necessary, approximately 60% of the time.

• Legal authorization to work in the country where the 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 schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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