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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: R1601398
Company:
Bristol Myers Squibb
Location: Hyderabad, Telangana, India
Employment Type: Full-Time
Function: Global Clinical Development / Trial Operations


Position Overview

The Senior Global Trial Acceleration Associate supports global clinical trial operations with a focus on accelerating study start-up, improving site activation timelines, and ensuring smooth execution of clinical development processes. The role works closely with cross-functional teams and external partners to ensure timely and compliant trial delivery.


Core Responsibilities

Trial Start-Up & Acceleration

  • Support rapid initiation of clinical trials across global programs

  • Track and drive completion of start-up deliverables and milestones

  • Identify delays in study start-up and support resolution of blockers

  • Coordinate submission and approval processes for study initiation


Site Activation & Study Coordination

  • Support site identification, selection, and activation processes

  • Monitor site readiness and ensure timely activation

  • Coordinate with CROs, investigators, and internal teams

  • Assist in resolving site-level operational issues


Cross-Functional Collaboration

  • Work with Clinical Operations, Regulatory, Ethics Committees, and Quality teams

  • Coordinate between global and regional stakeholders for study alignment

  • Support communication with CROs and external vendors

  • Ensure consistent execution across regions and studies


Documentation & Compliance

  • Maintain accurate and complete study start-up documentation

  • Ensure compliance with:

    • Good Clinical Practice (GCP)

    • Regulatory requirements

    • Internal SOPs and quality standards

  • Support audit and inspection readiness activities


Tracking & Reporting

  • Maintain study trackers for start-up and activation progress

  • Provide regular updates to study teams and leadership

  • Ensure accurate data entry in clinical systems (e.g., CTMS)

  • Monitor and report key performance indicators (KPIs)


Process Improvement

  • Identify inefficiencies in trial start-up workflows

  • Support continuous improvement initiatives

  • Contribute to standardization of global processes

  • Recommend solutions to improve trial acceleration timelines


Minimum Qualifications

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field

Experience

  • Experience in clinical research or pharmaceutical industry preferred

  • Exposure to clinical trial start-up or site management is an advantage


Key Skills & Competencies

Clinical & Operational Skills

  • Clinical Trial Start-Up

  • Site Activation & Feasibility

  • GCP & Regulatory Compliance

  • Clinical Documentation Management

  • Study Tracking (CTMS preferred)


Project Coordination

  • Timeline & milestone management

  • Cross-functional coordination

  • CRO/vendor collaboration

  • Process improvement mindset


Technical Skills

  • Microsoft Office (Excel, PowerPoint, Word, Teams)

  • Clinical systems (CTMS, eTMF preferred)

  • Data tracking and reporting tools


Soft Skills

  • Strong attention to detail

  • Organizational ability

  • Communication and stakeholder management

  • Problem-solving in fast-paced environments

  • Ability to work in global matrix teams


Role Focus

  • Clinical Trial Operations

  • Study Start-Up & Acceleration

  • Site Activation & Monitoring Support

  • Global Clinical Development Coordination