Clinical Research Associate I

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

📋 Description

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

• Provide precise status reports for studies and maintain thorough documentation.

• Efficiently manage queries generated by sponsors.

• Take charge of ensuring cost efficiency throughout the study.

• Contribute to the preparation and assessment of study documentation and feasibility analyses for new proposals.

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

• Guarantee patient safety and adherence to ICON procedures, protocols, and regulatory standards.

⛳️ 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 effectively.

• Strong written and verbal communication skills in English.

• Good interpersonal skills to handle queries promptly.

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

• 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.