GlobalStudySupplySupport
Capgemini
GlobalStudySupplySupport
Job Description
GlobalStudySupplySupport
📋 Job Overview
As a Clinical Supply Chain Support Specialist at Capgemini in Hyderabad, you will provide operational support to study leaders for clinical trials across all phases, ensuring efficient supply chain management and regulatory compliance. The role involves independent work and collaboration with cross-functional teams to handle logistics, documentation, and quality processes. With 2-14 years of experience required, it offers a dynamic environment in the healthcare and life sciences sector.
📍 Location: Hyderabad
💼 Experience Level: Experienced Professionals
🏢 Business Unit: Engineering and RandD Services
🎯 Key Responsibilities
- Prepare and track transfer orders
- Manage stock reconciliation and monitor destruction needs
- Perform quality checks and maintain inspection readiness
- Prepare documentation for labeling and shipments
- Archive documents in the electronic Trial Master File
- Communicate effectively with supply chain leaders, operational teams, and outsourcing partners
- Adapt to changing priorities in a fast-paced environment
✅ Required Qualifications
- Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD)
- Experience in clinical supply support or logistics for clinical trials (Phase I–IV)
- Knowledge of regulatory standards (quality, safety, documentation)
- Understanding of investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction)
- Fluent English for communication with stakeholders
🛠️ Required Skills
- Proficiency with IRT tools (e.g., Endpoint, Suvoda)
- Proficiency with Smart Supplies
- Proficiency with Veeva Vault
- Strong documentation skills
- Strong quality check skills
- Attention to detail and organizational skills
- Ability to manage multiple priorities
- Collaborative skills in a multicultural environment
- Strong problem-solving skills
- Adaptability skills
- Comfort with digital tools and documentation processes
🎁 Benefits & Perks
- Remote work options
- Adaptable schedules for work-life balance
- Inclusive culture focused on growth, innovation, and excellence
- Continuous learning opportunities and certifications in emerging technologies and methodologies
Locations
- Hyderabad, India
Salary
Estimated Salary Rangemedium confidence
2,500,000 - 4,200,000 INR / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Proficiency with IRT tools (e.g., Endpoint, Suvoda)intermediate
- Proficiency with Smart Suppliesintermediate
- Proficiency with Veeva Vaultintermediate
- Strong documentation skillsintermediate
- Strong quality check skillsintermediate
- Attention to detail and organizational skillsintermediate
- Ability to manage multiple prioritiesintermediate
- Collaborative skills in a multicultural environmentintermediate
- Strong problem-solving skillsintermediate
- Adaptability skillsintermediate
- Comfort with digital tools and documentation processesintermediate
Required Qualifications
- Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD) (experience)
- Experience in clinical supply support or logistics for clinical trials (Phase I–IV) (experience)
- Knowledge of regulatory standards (quality, safety, documentation) (experience)
- Understanding of investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction) (experience)
- Fluent English for communication with stakeholders (experience)
Responsibilities
- Prepare and track transfer orders
- Manage stock reconciliation and monitor destruction needs
- Perform quality checks and maintain inspection readiness
- Prepare documentation for labeling and shipments
- Archive documents in the electronic Trial Master File
- Communicate effectively with supply chain leaders, operational teams, and outsourcing partners
- Adapt to changing priorities in a fast-paced environment
Benefits
- general: Remote work options
- general: Adaptable schedules for work-life balance
- general: Inclusive culture focused on growth, innovation, and excellence
- general: Continuous learning opportunities and certifications in emerging technologies and methodologies
Tags & Categories
Answer 10 quick questions to check your fit for GlobalStudySupplySupport @ Capgemini.
10 Questions
~2 Minutes
Instant Score
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GlobalStudySupplySupport
Capgemini
GlobalStudySupplySupport
Job Description
GlobalStudySupplySupport
📋 Job Overview
As a Clinical Supply Chain Support Specialist at Capgemini in Hyderabad, you will provide operational support to study leaders for clinical trials across all phases, ensuring efficient supply chain management and regulatory compliance. The role involves independent work and collaboration with cross-functional teams to handle logistics, documentation, and quality processes. With 2-14 years of experience required, it offers a dynamic environment in the healthcare and life sciences sector.
📍 Location: Hyderabad
💼 Experience Level: Experienced Professionals
🏢 Business Unit: Engineering and RandD Services
🎯 Key Responsibilities
- Prepare and track transfer orders
- Manage stock reconciliation and monitor destruction needs
- Perform quality checks and maintain inspection readiness
- Prepare documentation for labeling and shipments
- Archive documents in the electronic Trial Master File
- Communicate effectively with supply chain leaders, operational teams, and outsourcing partners
- Adapt to changing priorities in a fast-paced environment
✅ Required Qualifications
- Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD)
- Experience in clinical supply support or logistics for clinical trials (Phase I–IV)
- Knowledge of regulatory standards (quality, safety, documentation)
- Understanding of investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction)
- Fluent English for communication with stakeholders
🛠️ Required Skills
- Proficiency with IRT tools (e.g., Endpoint, Suvoda)
- Proficiency with Smart Supplies
- Proficiency with Veeva Vault
- Strong documentation skills
- Strong quality check skills
- Attention to detail and organizational skills
- Ability to manage multiple priorities
- Collaborative skills in a multicultural environment
- Strong problem-solving skills
- Adaptability skills
- Comfort with digital tools and documentation processes
🎁 Benefits & Perks
- Remote work options
- Adaptable schedules for work-life balance
- Inclusive culture focused on growth, innovation, and excellence
- Continuous learning opportunities and certifications in emerging technologies and methodologies
Locations
- Hyderabad, India
Salary
Estimated Salary Rangemedium confidence
2,500,000 - 4,200,000 INR / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Proficiency with IRT tools (e.g., Endpoint, Suvoda)intermediate
- Proficiency with Smart Suppliesintermediate
- Proficiency with Veeva Vaultintermediate
- Strong documentation skillsintermediate
- Strong quality check skillsintermediate
- Attention to detail and organizational skillsintermediate
- Ability to manage multiple prioritiesintermediate
- Collaborative skills in a multicultural environmentintermediate
- Strong problem-solving skillsintermediate
- Adaptability skillsintermediate
- Comfort with digital tools and documentation processesintermediate
Required Qualifications
- Pharmaceutical or health-related degree (Bac+3, Bac+5, or PhD) (experience)
- Experience in clinical supply support or logistics for clinical trials (Phase I–IV) (experience)
- Knowledge of regulatory standards (quality, safety, documentation) (experience)
- Understanding of investigational product management (kit types, shelf life, depot management, distribution, reconciliation, returns, destruction) (experience)
- Fluent English for communication with stakeholders (experience)
Responsibilities
- Prepare and track transfer orders
- Manage stock reconciliation and monitor destruction needs
- Perform quality checks and maintain inspection readiness
- Prepare documentation for labeling and shipments
- Archive documents in the electronic Trial Master File
- Communicate effectively with supply chain leaders, operational teams, and outsourcing partners
- Adapt to changing priorities in a fast-paced environment
Benefits
- general: Remote work options
- general: Adaptable schedules for work-life balance
- general: Inclusive culture focused on growth, innovation, and excellence
- general: Continuous learning opportunities and certifications in emerging technologies and methodologies
Tags & Categories
Answer 10 quick questions to check your fit for GlobalStudySupplySupport @ Capgemini.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs