Clinical Research Associate

This is a fully remote position, open to applicants in California, +1 more state.

📋 Description

• Oversee all tasks related to the establishment and monitoring of a study

• Accurately complete study status reports and uphold study documentation

• Efficiently manage sponsor-generated inquiries

• Ensure the cost-effectiveness of the study

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

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

• Ensure adherence to ICON's procedures, protocols, and regulatory standards to safeguard patient safety

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field

• Relevant experience in clinical trial monitoring

• Familiarity with ICH-GCP guidelines

• Ability to review and assess medical data

• Strong written and verbal communication skills in English

• Good interpersonal skills to address inquiries promptly

• Willingness to travel as necessary (approximately 60%)

• Legal eligibility 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 plans

• Life insurance and disability coverage

• Employee assistance programs and wellness resources

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