**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Job Title** Senior Global Trial Manager **Division** Research and Development **Functional Area Description** Global Trial Managers, crossing all therapeutic areas and research phases, collaborate with cross-functional teams to drive operational aspects of complex, global clinical research studies from concept to final clinical study report. **Position Summary / Objective** + Provides strategic and operational leadership of clinical research studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs. + Independently leads complex, large, global in-house or outsourced, Non- Registrational Data Generating or Registrational Data Generating trials/studies at any point in the life cycle of the trial/study (i.e. start up, maintenance, or close-out). + Acts as the primary operational contact for the study and leads the cross- functional global team for execution of the study. + May provide operational leadership of one or more cross-functional Study Team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. + Has high global organizational impact and influence, and significant impact on function and Study Team. **Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned.** **Position Responsibilities** **Responsibilities involve a combination of execution and oversight, dependent on the sourcing model, to ensure deliverables and may include, but are not limited to, the following:** **Project Management** + Directs and delegates to the assigned Global Trial Management Staff as applicable + Drives study execution utilizing available performance metrics and quality indicators and study milestones and drivers + Oversees clinical monitoring quality and adherence to established processes and plans. + Develops, manages, and maintains study deliverables (i.e. timelines, study plans, etc.) through collaboration with internal and external stakeholders using data and strong interpersonal influencing skills to make robust data driven decisions. + Proactively identifies potential risks and develops/implements actions to avoid/mitigate and make the appropriate trade-offs of balancing risks with study deliverables and costs. + Maintains/updates data as appropriate in project management tools including CTMS. + Troubleshoots complex issues with little guidance and support. + Informs operational program lead(s) and other leadership (as appropriate) on overall clinical trial plans, recruitment status, and raises potential issues/mitigation. + Leads, develops, and implements cross-functional/global initiatives and best practices. + Creates, maintains, and implements project management tools at the study level (e.g. actions, decisions, issues log and risk management plan). **Study Planning and Conduct** + Supports and oversees country and site feasibility/selection processes with use of robust data. + Provides operational and strategic input into Study Team and study documents. + Collaborates with CSO on global investigational product [IP] supply forecasting/management. + Participates in the subject recruitment/retention strategy and related initiatives (e.g. recruitment material). + Participates in clinical service provider (vendor) selection, specification development, and management/oversight. + Oversees TMF set-up, ongoing quality review, operational oversight memo, and requests final reconciliation. + Provides input to and reviews study training for Study Team, investigational sites, and vendors in collaboration with the Clinical Scientist. + Oversees study specific CSR appendices. + Provides input and communicates with the appropriate teams for response to country/regulatory and IRB/IEC. + Proactively manages issues and information sharing with key internal/external stakeholders with use of standardized reports and other mechanisms. + Highly proactive risk identification, contingency planning, innovative problem solving, and the ability to solve multiple problems with varying degrees of complexity for multiple functions and understands when escalation is needed. + Oversees service providers without supervision. + Leads Audit Response Team and CAPA and participates in inspections. + Supports the development/management/review vendor scope of work (SOW), invoices, and accruals as per the contract, quality requirements, and budget. **Relationship Management** + Proactively develops and maintains collaborative relationships with internal partners/stakeholders across the multidisciplinary teams. + Manages external partners including Contract Research Organizations (CROs), Academic Research Organizations (AROs), and other clinical service providers as applicable. + Influences key stakeholders inside/outside of the team and capitalizes on established relationships. **Leadership Competencies** + Creates realistic plans that clearly define goals, milestones, responsibilities and results. + Maintains focus on strategic objectives while accomplishing operational goals. + Places a priority on getting results with an emphasis on high quality outcomes. + Holds self and others accountable for accomplishing goals. + Makes timely, data-driven decisions while balancing against daily priorities. + Develops and maintains effective working relationships with people across cultures. + Encourages collaboration across teams, functions, and geographies. + Ensures that conflict is handled constructively so that performance is not impacted. + Displays a willingness to challenge the status quo and take risks. + Responds resourcefully to changing business demands and opportunities, proactively looking for ways the team can contribute. + Maintains optimism, support and composure in times of change, uncertainty, or stress. + Executes/delivers on corporate objectives and drives goals. + Leads global cross functional therapeutic programs. + Creates global solutions for processes. + Acts as mentor, driver, and motivator to Global Trial Specialist, Associate GTMs, GTMs, and others in the Study Team and function, especially during challenging times. + Frequently encourages others to consider new approaches and ideas, avoiding getting stuck in a "one right way" approach. + Models and promotes positive team behaviors in a cross-functional setting by inspiring and holding others accountable for accomplishing goals, building a culture of energy and commitment that challenges people to excel, recognizing and rewarding accomplishments, managing issues, and providing guidance/feedback on performance. + Can be viewed as a SME by cross functional teams. + May participate in company initiatives, leads continuous improvement initiatives, and shares knowledge where applicable. + Provides guidance regarding company policies and procedures. **Degree Requirements** BA/BS or equivalent degree in relevant discipline **Experience Requirements** + Minimum 6 years of clinical study management experience of which at least 2 years should have been in direct multinational study management. + Experience in leading global clinical trials and multi-functional teams. + Demonstrated project management and organizational skills with strong presentation and communication abilities. + Experience with electronic quality, compliance and CTMS systems. + Risk management experience preferred. + Experience in managing CROs experience is a plus. **Key Competency Requirements** + Demonstrated project management and organizational skills with strong presentation and communication abilities. + Ability to see and understand how work at hand may have program or global implications and follows through to connect appropriate stakeholders **Technical Competencies** + Strategic clinical trial project management and study management expert. + Intermediate knowledge of clinical trial forecasting, and financial management. + Expert knowledge of ICH/GCP, regulatory guidelines/directives, and drug development and Clinical Trial Process (CTP). + Expert level cross functional awareness. + Proven success in using oral/written communication skills to influence, inform, or guide others. + Fosters a continuous learning mindset. + Computer skills - Microsoft applications including (but not limited to), Word, Excel, PowerPoint. + Proficiency in study tools including electronic system skills - e.g. CTMS / eTMF **Management Competencies** + Leadership/influence and negotiating management skills. + Ability to effectively lead a cross-functional team in a matrix environment. + Time management skills - ability to effectively multi-task and set priorities for self and assists others with the same. + Has the command of the projects, the ability to zoom in and out as the situation demands and deliver high quality presentations to senior and executive leadership within and outside of BMS (as appropriate). + Has critical thinking skills for problem solving and the lateral and strategic thinking capacity to drive the study(ies) and understanding the upstream, downstream and lateral implications of decisions that affect study outcomes and timelines. + Proven problem-solving skills to address and overcome complex safety and compliance related issues during clinical program implementation and execution. + Excellent negotiating and influencing skills. + Adaptable and flexible-willing/able to adjust to multiple demands and shifting priorities and demonstrates ability to meet day-to-day challenges with confidence and professionalism. **Travel Required** Up to 25% If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. **Uniquely Interesting Work, Life-changing Careers** With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. **On-site Protocol** BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. **Company:** Bristol-Myers Squibb **Req Number:** R1579366 **Updated:** 2024-12-24 03:19:52.264 UTC **Location:** Hyderabad-IN Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.