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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

As a Global Trial Specialist, you will support the planning, execution, and management of global clinical trials. This includes assisting with study startup, maintenance, and closeout activities, coordinating vendors, ensuring regulatory compliance, and facilitating communication across global study teams.


⚙️ Key Responsibilities

Study/Project Planning, Conduct & Management

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

  • Support Global Trial Manager (GTM) and study teams in responding to country/regulatory and IRB/IEC queries.

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

  • Assist GTM in driving study execution and escalation of potential issues.

  • Facilitate vendor creation and payment processing with appropriate stakeholders.

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

  • Manage global vendor site lists and resolve related issues.

  • Maintain study mail-groups, distributions, SharePoint, and Study Directory updates.

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

  • Identify study risks and develop mitigation strategies, escalating as needed.

  • Participate in filing activities and audits, as applicable.


🎓 Qualifications & Experience

Technical Competencies

  • Basic knowledge of clinical research budgets, including processing, reporting, and vendor payments (preferred).

  • Familiarity with ICH/GCP guidelines and regulatory directives.

  • Basic understanding of project management principles (desired).

Management Competencies

  • Ability to build relationships with key stakeholders across study teams.

  • Flexibility to adapt to changing business demands and proactively contribute.

  • Willingness to challenge the status quo and take initiative.

  • Strong oral and written communication skills.

  • Ability to collaborate effectively across the organization.

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 (preferred).

  • Global clinical trial experience (a plus).

  • Travel: <5%.


🌍 Work Environment & Culture

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

  • Employees are empowered to apply their unique 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: Ability to travel for work-related visits and meetings


⚖️ Equal Employment Opportunity & Safety

  • BMS ensures accessibility and 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 processed in recruitment is handled per applicable privacy policies.