Senior Clinical Research Associate - Remote

Overview

The Senior Clinical Research Associate (CRA) is responsible for monitoring Phase I-IV Pharma clinical trials, ensuring compliance with regulations and delivering quality data while working remotely.

In Short

• Remote position requiring travel up to 80% of the time.
• Primary site manager for clinical investigative sites.
• Facilitates trial initiation and conducts monitoring activities.
• Ensures compliance with ICH/GCP and US CFR regulations.
• Delivers timely and quality data for clinical trials.
• Collaborates with internal stakeholders and site personnel.
• Requires a BS/BA degree in a scientific or healthcare discipline.
• Minimum of 3 years of site monitoring experience preferred.
• Oncology and Neuroscience experience highly desirable.
• Strong communication and problem-solving skills required.

Requirements

• BS/BA degree in a scientific or healthcare discipline.
• Minimum of 3 years of experience in site monitoring.
• Strong understanding of clinical trial processes.
• Knowledge of GCP/ICH and FDA regulations.
• Excellent communication and presentation skills.
• Ability to manage multiple priorities effectively.
• Fluency in English required.
• Experience in Oncology or Neuroscience is a plus.
• Driving is an essential function of this role.
• Must have a valid driver’s license.

Benefits

• Comprehensive benefits package including health and life insurance.
• 401(k) with company contribution and match.
• Generous time off package including vacation and personal days.
• Performance-based cash incentive.
• Eligibility for annual equity awards depending on role level.