Clinical Research Associate

This is a fully remote position, open to applicants in New Jersey, +2 more states.

📋 Description

• Oversee all tasks associated with the setup and monitoring of a clinical study.

• Produce precise study status reports and uphold study documentation.

• Efficiently manage sponsor-generated queries and ensure study cost-effectiveness.

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

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

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

• Provide clinical trial monitoring services to a high standard across various clinical programs.

⛳️ Requirements

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

• Relevant experience in clinical trial monitoring.

• Preferred experience in monitoring Ophthalmology trials or multi-TA as specified by the client.

• Familiarity with ICH-GCP guidelines.

• Proficiency in reviewing and assessing medical data.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills for effectively addressing queries.

• 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.

• Performance-based incentives.

• 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.