Senior Associate, Clinical Research - Remote

Overview

The Senior Associate, Clinical Research will act as a customer advocate through the study life cycle, ensuring compliance with study protocols and regulatory requirements while supporting clinical operations.

In Short

• Act as a customer advocate through the study life cycle.
• Support study goals in alignment with corporate objectives.
• Organize and maintain clinical study documentation.
• Monitor clinical sites and ensure compliance with protocols.
• Provide oversight of CRO monitoring activities.
• Assist in developing study-specific monitoring procedures.
• Review and develop study-related documents.
• Train study staff in GCP and protocol procedures.
• Ensure patient protection and data integrity.
• Prepare trip and audit reports in accordance with GCP.

Requirements

• Bachelor’s degree in life sciences or related field.
• Minimum of five years of clinical research monitoring experience.
• Experience in pharmaceutical and ophthalmology sectors.
• Knowledge of ICH/GCP R2 Guidelines.
• Ability to work with minimal supervision.
• Strong problem-solving and prioritization skills.
• Mentoring experience preferred.
• Proficient in MS Office and clinical trials software.
• Professional interaction skills across organizational levels.
• Ability to manage competing priorities in a fast-paced environment.

Benefits

• Hybrid work environment with remote options.
• Comprehensive health, dental, and vision insurance.
• Generous paid time off including vacation and personal days.
• Bonus and stock equity opportunities.
• Supportive company culture focused on innovation and teamwork.