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Sr Global Trial Acceleration Associate

Bristol Myers Squibb
2+ years
Not Disclosed
Hyderabad
10 June 9, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategies, Data Visualization, Machine Learning (ML), Master Da, Auditing, Audit Management, Audits Compliance, Communication, Continued Learning, Decision Making, Gmp Procedures, Inspection Readiness, Managing Ambiguity, Organizing, People Management and Leadershi, Bachelor’s Degree (BS) or Master’s Degree (MS) in: Life Sciences Pharmacy Biotechnology Biomedical Sciences Chemistry Regulatory Affairs Or related scientific disciplines, Budget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Causality Assessment, Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, Clinical Research, Clinical Trials, Curious Mindset, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Pat, Clinical SAS Programming, Clinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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