Global Study Supply Support Jobs

Job description
Job Requirements

Global Study Supply Support Jobs in Hyderabad at Capgemini

Job Title: Global Study Supply Support (GSSS)

Company Name: Capgemini

Location: Hyderabad, Telangana

Qualification: Any Graduate

Experience: Relevant experience in Clinical Trials / Supply Chain / GxP preferred

Salary: Best in Industry

Employment Type: Full Time, Permanent

Industry: IT Services & Consulting

Department: Healthcare & Life Sciences

Role Category: Healthcare & Life Sciences – Other

Job Description:

Capgemini is seeking a detail-oriented and proactive Global Study Supply Support (GSSS) professional to join its Healthcare & Life Sciences division in Hyderabad. As part of the clinical supply chain operations, the GSSS supports Clinical Supply Chain Study Leaders (CSC SL) across multiple Phase I–IV studies. This role requires strong understanding of clinical trial processes, investigational product (IP) management, regulatory requirements, and coordination within cross-functional teams.

You will be responsible for supporting study setup, follow-up, and close-out activities by managing transfer orders, inventory tracking, documentation, reconciliation, and shipment coordination. The role includes working with industry-standard clinical tools such as eTMF, Veeva Vault, RAID, IRT systems, and temperature excursion management platforms. The GSSS ensures high-quality, timely, and compliant supply chain execution throughout a study’s lifecycle.

This position is ideal for candidates who thrive in a structured, compliance-driven environment and are eager to contribute to global clinical operations. With Capgemini’s strong digital and technological ecosystem, this role offers excellent exposure, continuous learning, and long-term career growth.

Roles & Responsibilities:

• Create, track, and follow up Transfer Orders (TF) in supply management systems

• Manage IPTT, IP reconciliation, stock updates, and corporate-level reconciliation

• Perform quality checks on documentation and supply-related data

• Prepare documents for labeling, shipments, and IMP transfers

• File required study documents in eTMF and ensure inspection readiness

• Support mandatory shipment documentation and CSPO management

• Enter shipment orders, assist CSC SL with shipment tracking and stock monitoring

• Manage destruction of expired IMP and coordinate destruction certificates

• Monitor IRT interface failures and alert CSC SL as needed

• Extract temperature excursion data and support KPI tracking

• Manage purchase orders, vendor invoices, and financial documentation

• Ensure compliance with GxP, clinical supply standards, and SOPs

Benefits:

• Opportunity to work with a global industry leader

• Exposure to advanced clinical tools (Veeva, IRT, RAID, TEX)

• Professional development in clinical operations & supply chain

• Collaborative and diverse work culture

• Long-term career growth in a stable, tech-driven environment

Additional Information:

• Preferred skills: Veeva Vault, IRT systems, Clinical Trials, Supply Chain, GxP

• Strong communication, organizational skills, and attention to detail required