Senior Clinical Research Associate (Remote)

Overview

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

In Short

• Join our A-team as a Senior Clinical Research Associate (Sr.CRA) in a remote position.
• Independently control and monitor investigational sites.
• Detect issues proactively and provide solutions for clinical study compliance.
• Governs quality standards for trial monitoring activities.
• Conducts study tasks in compliance with quality and efficiency.
• Monitors activities at clinical study sites for adherence to protocols.
• Prepares and submits Site Visits Reports and Contact reports.
• Maintains CTMS in compliance with SOPs and directives.
• Acts as Document Owner for collected study documents.
• Tracks ongoing study data for project status reporting.

Requirements

• Experience in clinical research monitoring.
• Knowledge of ICH, GCP, SOPs, and applicable regulations.
• Strong organizational and communication skills.
• Ability to manage multiple studies simultaneously.
• Proficient in CTMS and study documentation management.
• Experience in site management and monitoring.
• Ability to identify and resolve logistical problems.
• Experience in preparing for audits and inspections.
• Collaborative mindset to work with project teams and sponsors.
• Ability to generate status updates and progress reports.

Benefits

• Work remotely from anywhere.
• Opportunity to work with a dedicated team in biopharmaceuticals.
• Engage in meaningful work that impacts patient care.
• Flexible working hours.
• Competitive compensation.
• Professional growth and development opportunities.
• Collaborative work environment.
• Access to industry-leading resources and tools.