Senior Regulatory Compliance Coordinator

📋 Description

• Manage regulatory components of cancer clinical trials from initiation to closure.
• Ensure regulatory integrity and accuracy of trial documentation and submissions.
• Collaborate with investigators and teams during development and start-up phases.
• Serve as primary regulatory contact during protocol development and submissions.
• Coordinate IRB submissions and reviews.
• Support regulatory and safety documentation submissions to sponsors and agencies.

🎯 Requirements

• Experience in clinical research, regulatory affairs, or related field.
• Understanding of regulatory processes for clinical research and cancer trials.
• Experience preparing IRB submissions and regulatory/safety reports.
• Ability to manage studies through submission, approval, maintenance, amendment, and closure.
• Experience collaborating with investigators and multidisciplinary teams.
• Strong organizational and project coordination skills.

🎁 Benefits

• Senior-level role with regulatory oversight and staff mentorship.
• Opportunity to contribute to cancer clinical trials and research initiatives.
• Exposure to diverse trial portfolios and cross-functional collaboration.
• Professional growth in clinical trial regulatory operations and compliance.
• Mentoring responsibilities and team-oriented environment.