Instagram
youtube
Facebook

Global Trial Specialist

3+ years
Not Disclosed
10 Oct. 4, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🏷️ Job Title: Global Trial Specialist

📍 Location: Hyderabad, Telangana, India
🕒 Employment Type: Full Time
🏢 Company: Bristol Myers Squibb (BMS)


🧭 Position Overview

The Global Trial Specialist supports global clinical trial operations, including study planning, execution, and management. The role involves facilitating study startup, maintenance, and closeout activities, coordinating vendors, ensuring regulatory compliance, and supporting global study teams.


⚙️ Key Responsibilities

Study/Project Planning & Management

  • Understand study-level tools, plans, and protocols.

  • Support Global Trial Manager (GTM) and study teams for regulatory, country, and IRB/IEC responses.

  • Participate in operational processes for study startup, maintenance, and closeout.

  • Assist GTM in driving study execution and escalate issues as appropriate.

  • Facilitate vendor creation, payment processing, and issue resolution.

  • Develop, update, and submit Transfer of Obligations to Regulatory Authorities.

  • Manage global vendor site lists, study mail-groups, SharePoint, and Study Directory updates.

  • Organize study team meetings, set agendas, and capture meeting minutes.

  • Identify risks, develop mitigations, and escalate as needed.

  • Support filing activities and audits as applicable.


🎓 Qualifications & Experience

Technical Competencies

  • Knowledge of ICH/GCP and regulatory guidelines.

  • Basic understanding of clinical research budgets (processing, reporting, tracking).

  • Basic understanding of project management (desired).

Management Competencies

  • Ability to build relationships with stakeholders across study teams.

  • Flexible and proactive approach to changing business demands.

  • Willingness to challenge the status quo and take initiative.

  • Strong oral and written communication skills.

  • Collaboration skills across teams and functions.

Education & Experience

  • BA/BS or Associate degree in a relevant discipline.

  • 3+ years’ experience with Clinical Trial Management Systems (CTMS) and Clinical Trial Master File (CTMF) systems (preferred).

  • Experience in clinical research or related work is a plus.

  • Global clinical trial experience is a plus.

  • Travel: <5%.


🌍 Work Environment & Culture

  • BMS emphasizes challenging, meaningful, and life-changing work.

  • Employees are empowered to apply their talents in a supportive culture.

  • 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 as required for meetings, customers, and patients


⚖️ Equal Employment & Safety

  • BMS provides accommodations for people with disabilities.

  • Applicants with arrest or conviction records are considered per local laws.

  • Employees are strongly encouraged to maintain up-to-date COVID-19 vaccinations.

  • Data in recruitment is processed according to privacy policies.