Global Trial Specialist

As a member of the Bristol Myers Squibb team, you will be part of a challenging, meaningful, and life-changing work environment where unique and interesting work happens every day. From optimizing production lines to making breakthroughs in cell therapy, your work will have a transformative impact on the lives of patients and your career growth opportunities will be unmatched. **Key Responsibilities:** - Study/Project Planning, Conduct, and Management - Understand study level tools and plans. - Provide support to the GTM for response to country/regulatory and IRB/IEC. - Assist in driving study execution. - Manage global vendor site lists and resolve related issues. - Participate in filing activities and associated audits as applicable. **Qualifications:** - **Technical Competencies:** - Knowledge of ICH/GCP and regulatory guidelines/directives. - Basic understanding of project management is desired. - **Management Competencies:** - Begin networking and fostering relationships with key stakeholders. - Respond flexibly to changing business demands and opportunities. - Display willingness to challenge the status quo and take risks. - Effective oral/written communication skills. If a role at Bristol Myers Squibb intrigues you, even if it doesn't perfectly align with your resume, we encourage you to apply. You could be on the brink of a career that will transform your life and make a significant impact on patient care. At Bristol Myers Squibb, every employee contributes to the vision of transforming patients" lives through science. The company values individual talents, unique perspectives, and a supportive culture that promotes global participation in clinical trials. If you are dedicated to making a difference and are looking for a challenging yet rewarding career, Bristol Myers Squibb is the place for you.,