Pharma Job at Capgemini | Apply Now for the Global Study Supply Support Role
Capgemini is seeking a motivated professional for the Global Study Supply Support (GSSS) role to provide essential operational assistance to Clinical Supply Chain Study Leaders. This Pharma Job requires 2+ years of experience in clinical supply logistics and a Pharmaceutical or health-related degree. The GSSS specialist will be responsible for critical activities across all trial phases, including managing stock reconciliation, preparing documentation for labeling/shipments, using advanced systems like IRT and Veeva Vault, and ensuring strict compliance with regulatory standards for Investigational Product management at Capgemini.
- Job Title: Global Study Supply Support (GSSS)
- Location: Hyderabad
About Capgemini
Capgemini is a global leader in partnering with companies to transform and manage their business by harnessing the power of technology. As a prominent multinational corporation, Capgemini offers a broad spectrum of services, including consulting, technology, and outsourcing. Within the Life Sciences sector, Capgemini provides specialized support, such as managing complex global operations like the Clinical Supply Chain, ensuring clients adhere to stringent regulatory standards and effectively utilize advanced digital tools (like IRT and Veeva Vault) to support clinical trials worldwide.
Capgemini Job Overview
Provide operational support to Clinical Supply Chain Study Leaders for multiple studies across all phases (set-up, follow-up, closure). Work independently and collaborate with multiple leaders and cross-functional teams. Prepare and track transfer orders, manage stock reconciliation, perform quality checks, prepare documentation for labeling and shipments, monitor needs for destruction, and archive documents in the electronic Trial Master File.
Key Responsibilities of the Capgemini Job
- Support clinical supply chain operations for global studies.
- Ensure compliance with regulatory standards and protocols.
- Maintain accurate documentation and inspection readiness.
- Communicate effectively with supply chain leaders, operational teams, and outsourcing partners.
- Adapt to changing priorities in a fast-paced environment.
Must-Have Skills & Qualifications
- Education: Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD).
- Clinical supply support or logistics for clinical trials (Phase I-IV).
- Digital tools and supply chain software.
- Regulatory standards (quality, safety, documentation).
- Investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction).
- Proficiency with tools: IRT (e.g., Endpoint, Suvoda), Smart Supplies, Veeva Vault.
- Documentation and quality check skills.
- Fluent English for communication with stakeholders.
Key Competencies
- Attention to detail and organizational skills.
- Ability to manage multiple priorities and work collaboratively in a multicultural environment.
- Strong problem-solving and adaptability skills.
- Comfort with digital tools and documentation processes.
