Clinical Research Associate I - Remote

Overview

As a Clinical Research Associate I at Ora, you will develop strong clinical site relationships and ensure compliance with study protocols while working under the oversight of Lead CRAs and Line Managers.

In Short

• Develop strong site relationships throughout all phases of the trial.
• Perform clinical study site management and monitoring activities.
• Gain in-depth understanding of study protocols.
• Coordinate tasks with internal roles for site readiness.
• Participate in site selection and validation activities.
• Conduct remote and on-site monitoring activities.
• Ensure data accuracy and subject safety.
• Collect and review regulatory documentation.
• Communicate with investigators on protocol conduct issues.
• Support audit and inspection activities as needed.

Requirements

• Bachelor's degree with 1 year of clinical research experience.
• Ophthalmic experience preferred.
• Ability to assess protocol and GCP compliance.
• Strong attention to detail.
• Knowledge of federal regulations governing research.
• Proficiency with Excel, CTMS, and EDC.
• Multilingual communication is a plus.

Benefits

• Comprehensive healthcare options from day 1.
• Flexible PTO and unlimited sick time.
• Competitive salaries with a 401K plan.
• Adoption and fertility assistance.
• Company paid life and disability insurance.
• Remote workspace reimbursement.
• Employee assistance program.
• Career development opportunities.
• Global team collaboration.
• Impactful research opportunities.