Senior Clinical Research Associate Contractor - 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

• Provide functional assistance to project team members with administrative, logistical and practical issues.
• Track and supervise collection of ongoing study data for project status reporting.
• Assist in conducting feasibility assessments for potential studies.
• Govern minimum quality standards for trial monitoring activities.
• Monitor activities at clinical study sites for adherence to GCP, ICH, SOPs, and study protocols.
• Prepare site visit and telephone reports.
• Responsible for multiple projects, working independently and in a team environment.
• May participate in study development and start-up processes.
• Resolve site issues and determine status for IP shipment.
• Train, mentor and/or supervise junior staff.

Requirements

• Experience in clinical research and monitoring.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Strong organizational and communication skills.
• Ability to work independently and manage multiple projects.
• Experience in training and mentoring junior staff.

Benefits

• Opportunity to work with a dedicated team in the biopharmaceutical industry.
• Flexible working environment.
• Engagement in meaningful work that impacts patient care.
• Professional development opportunities.