Sr Global Trial Acceleration Associate
Job ID: R1601397
Company: Bristol Myers Squibb
Location: Hyderabad, Telangana, India
Employment Type: Full-Time
Function: Clinical Trial Operations / Global Development Operations
Position Summary
The Senior Global Trial Acceleration Associate supports clinical trial execution by accelerating study start-up and operational processes across global development programs. The role focuses on improving trial timelines, coordinating cross-functional stakeholders, ensuring documentation readiness, and supporting efficient site activation and study delivery.
Key Responsibilities
Clinical Trial Start-Up & Acceleration
Support end-to-end clinical trial start-up activities to enable faster study activation.
Coordinate key start-up deliverables including documentation, approvals, and site readiness.
Track and manage study timelines to ensure timely execution of critical milestones.
Identify and address bottlenecks in trial initiation processes.
Cross-Functional Coordination
Collaborate with Clinical Operations, Regulatory Affairs, Ethics Committees, and study teams.
Work closely with global and regional stakeholders to align study requirements.
Support communication between internal teams, CROs, and external vendors.
Ensure alignment of trial start-up activities across geographies.
Document & Compliance Support
Ensure accuracy and completeness of study start-up documentation.
Support preparation and tracking of essential clinical trial documents.
Assist in maintaining compliance with:
Good Clinical Practice (GCP)
Regulatory requirements
Internal SOPs
Support audit readiness by ensuring documentation traceability.
Site Activation Support
Assist in site identification and activation workflows.
Track site readiness and activation status across studies.
Support resolution of site-level operational issues impacting activation timelines.
Coordinate with CROs and site teams to ensure smooth initiation processes.
Process Optimization
Identify opportunities to improve trial acceleration processes.
Support implementation of best practices for study start-up efficiency.
Contribute to continuous improvement initiatives within global trial operations.
Assist in standardization of processes across studies and regions.
Reporting & Tracking
Maintain trackers for study start-up progress and milestone completion.
Provide updates on study status to project teams and leadership.
Support data accuracy in clinical trial management systems.
Minimum Requirements
Education
Bachelor’s degree in life sciences, pharmacy, or related scientific discipline.
Experience
Prior experience in clinical trial operations, clinical research, or pharmaceutical industry preferred.
Exposure to study start-up or clinical trial coordination is an advantage.
Key Skills & Competencies
Clinical Operations Skills
Clinical Trial Start-Up
Site Activation & Feasibility
Regulatory & Ethics Processes
Study Documentation Management
GCP Compliance
Project & Coordination Skills
Timeline Tracking & Management
Cross-functional Collaboration
Vendor/CRO Coordination
Process Improvement
Technical Skills
Clinical Trial Systems (CTMS preferred)
Microsoft Office (Excel, Word, Teams)
Data tracking and reporting tools
Soft Skills
Strong organizational ability
Attention to detail
Problem-solving mindset
Communication and stakeholder management
Ability to work in fast-paced global environments
Ideal Candidate Profile
Early to mid-career clinical operations professional.
Strong interest in accelerating clinical trial timelines and operational excellence.
Comfortable working in global, matrixed environments.
Detail-oriented with strong coordination and tracking abilities.
Motivated by process improvement and efficiency in clinical research.
Career Focus Areas
Clinical Trial Operations
Study Start-Up & Site Activation
Global Clinical Development Support
CRO & Vendor Coordination
Trial Process Optimization
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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Remote, India | Siliguri |Illinois :
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