Clinical Trials Manager, Oncology - Remote

Overview

The Clinical Trials Manager for Oncology at Gilead is responsible for managing global clinical trials, ensuring compliance with regulatory guidelines, and delivering high-quality clinical data.

In Short

• Manage a global clinical Phase 2 Master Protocol Platform Study.
• Lead cross-functional teams to meet trial objectives.
• Develop operational plans and training materials.
• Ensure compliance with regulatory standards.
• Engage in Risk Based Quality Management activities.
• Oversee clinical vendor performance metrics.
• Collaborate with Regulatory for submission packages.
• Track and communicate study progress to management.
• Foster an inclusive and empowering team environment.
• Contribute to clinical systems development.

Requirements

• Bachelor's Degree with 5 years of experience or Master's Degree with 3 years of experience.
• Ability to manage full cycle study management.
• Excellent teamwork and communication skills.
• Thorough knowledge of FDA and EMA regulations.
• Advanced knowledge of study management best practices.
• Experience with MS Office Suite (Word, PowerPoint, Excel).
• Knowledge of Master Protocol Platform Study design is preferred.
• Global clinical trial experience in Oncology is a plus.
• Experience with project management tools like MS Project.
• Demonstrated leadership and team development ability.

Benefits

• Competitive salary and discretionary bonuses.
• Company-sponsored medical, dental, vision, and life insurance.
• Paid time off and benefits package.
• Inclusive work environment promoting diversity.
• Opportunities for professional development and career growth.
• Supportive leadership focused on employee empowerment.
• Commitment to equal employment opportunities.
• Access to employee assistance programs.
• Flexible working arrangements available.
• Engagement in community and social responsibility initiatives.