Job Opportunity: Global Study Supply Support Professional – Capgemini, Hyderabad

Job Summary

Capgemini is seeking a detail-oriented and proactive Global Study Supply Support Professional to join our team in Hyderabad. This position is ideal for candidates with 2–5 years of experience in the pharmaceutical or clinical research industry. In this role, you will be responsible for managing clinical trial supply chain operations, ensuring regulatory compliance, and facilitating the smooth movement of investigational products. You will gain extensive exposure to global Phase I–IV clinical studies, working within a collaborative, fast-paced international environment.

Job Overview

• Company: Capgemini
• Role: Global Study Supply Support Professional
• Location: Hyderabad, India
• Experience: 2–5 Years
• Employment Type: Full-Time
• Industry: Clinical Research / Pharmaceutical Supply Chain

Key Responsibilities

As a Global Study Supply Support Professional, you will play a critical role in the end-to-end management of clinical supplies. Your core responsibilities include:

• Supply Chain Management: Prepare and track clinical trial transfer orders and coordinate the distribution of investigational products.
• Inventory Oversight: Manage stock reconciliation, monitor inventory levels, and handle returns, destruction, and depot management activities.
• Documentation & Compliance: Ensure all activities adhere to GxP and regulatory standards. Maintain accurate records in the electronic Trial Master File (eTMF) and support the preparation of shipping and packaging documentation.
• Quality Assurance: Perform quality checks and support inspection readiness activities to ensure the highest standards of operational integrity.
• Stakeholder Coordination: Collaborate effectively with clinical supply chain teams, vendors, and global stakeholders to ensure seamless study execution.
• Adaptability: Efficiently manage changing priorities in a dynamic, fast-paced global environment.

Required Qualifications

• Educational Background: A degree in Pharmaceutical Sciences, Life Sciences, or a related healthcare field.
• Professional Experience: 2–5 years of proven experience in clinical supply chain operations or logistics, preferably involving Phase I–IV clinical trials.
• Regulatory Knowledge: Strong understanding of GxP, regulatory compliance, and international documentation standards.
• Operational Expertise: Familiarity with the investigational product lifecycle, including kit management, distribution, and reconciliation processes.
• Communication: Excellent written and verbal communication skills, with the ability to maintain meticulous documentation.

Technical Skills

Candidates must be proficient or have significant exposure to the following systems and tools:

• IRT Systems: Hands-on experience with systems like Endpoint or Suvoda.
• Supply Chain Platforms: Experience with Smart Supplies.
• Document Management: Proficiency in Veeva Vault (eTMF) and related clinical documentation systems.

Benefits & Perks

Working at Capgemini offers more than just a job; it offers a pathway to professional growth. Benefits include:

• Global Exposure: Opportunity to work on international clinical trials and collaborate with diverse, multinational teams.
• Professional Development: Access to structured learning programs and continuous skill-building initiatives.
• Comprehensive Benefits: Competitive compensation package, health insurance, transportation, and onsite cafeteria facilities.
• Brand Value: Benefit from the reputation and stability of a global industry leader.

Salary Insight

The estimated salary for this position ranges from ₹4.4 – ₹6.5 LPA, commensurate with your experience and current market standards.

How to Apply

If you meet the requirements and are ready to advance your career in the clinical supply chain sector, we encourage you to apply. Please visit the official company careers portal or the direct application link provided by our recruitment partners to submit your resume and cover letter.

We look forward to reviewing your application and discussing how your expertise can contribute to our global clinical supply operations.