🏷️ Job Title
Senior Global Trial Specialist
📍 Location: Hyderabad, Telangana, India
🏢 Company: Bristol Myers Squibb (BMS)
🕒 Employment Type: Full-time
🧭 Position Overview
The Senior Global Trial Specialist provides operational expertise and leadership to support clinical trials across start-up, maintenance, and close-out phases. The role focuses on project management, risk mitigation, study execution, vendor oversight, and cross-functional collaboration.
⚙️ Key Responsibilities
Project Management
Facilitate operational processes as a Subject Matter Expert (SME) for study start-up, maintenance, and closure.
Use performance metrics and quality indicators to support the Global Trial Manager in driving study execution.
Identify risks proactively and implement mitigation strategies.
Resolve routine issues and escalate critical matters appropriately.
Actively contribute as a key functional member on cross-functional teams.
Study/Project Planning & Execution
Provide input to study-level tools and plans with moderate supervision.
Independently perform core GTS tasks, escalating, delegating, or pushing back when necessary.
Lead components of study meetings as appropriate.
Oversee country regulatory (CTA, MoH) and country/site IRB/IEC approvals and notifications.
Flexibly manage multiple trials of varying stages and complexity.
Understand program-level strategy and its impact on individual studies.
Contribute to process development and improvement initiatives.
Assess situations and determine appropriate paths forward using available resources.
Understand interdependencies of assigned tasks.
Manage vendors and site payment processing/tracking.
Maintain study budget tracking tools, reconcile invoices, and support finance reporting.
🎓 Qualifications & Experience
Education
BA/BS in a relevant discipline strongly preferred.
Experience
Minimum 6+ years in Clinical Research or related work.
Experience with industry Clinical Trial Management Systems (CTMS) and Clinical Trial Master File Systems (CTMF).
Technical Competencies
Knowledge of ICH/GCP, regulatory guidelines/directives, and the drug development process.
Familiarity with clinical research budgets, including site/vendor payment tracking.
Working knowledge of project management is preferred.
Management Competencies
Network and foster relationships across study teams.
Respond flexibly to changing business demands.
Act as a role model for change and support cross-functional initiatives.
Mentor and coach team members where applicable.
Build collaborative relationships with internal and external stakeholders.
Demonstrate willingness to challenge the status quo and take calculated risks.
Strong oral/written communication and presentation skills.
Travel
Less than 5%
🌍 Work Culture & Environment
BMS empowers employees to contribute to global clinical trials and patient outcomes.
Core values: Passion, Innovation, Urgency, Accountability, Inclusion, Integrity.
🏢 On-site Protocol
Site-essential: 100% onsite
Site-by-design: Hybrid (≥50% onsite)
Field-based/Remote-by-design: Travel required for meetings, customers, and patients
⚖️ Equal Opportunity & Safety
BMS ensures accommodations for people with disabilities.
Applicants with arrest or conviction records are considered per local laws.
Employees encouraged to maintain COVID-19 vaccination and boosters.
Recruitment data handled per privacy regulations.
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