The Clinical Supplies Specialist job at Alvotech is an excellent opportunity for professionals with experience in clinical trial supply chain management, biosimilars, and biologics development. Alvotech, a global biopharmaceutical company focused on biosimilar medicines, is hiring a Clinical Supplies Specialist to support clinical trial supply planning, forecasting, packaging, labeling, and distribution activities.
This clinical supply management job in Bangalore requires 2โ5 years of experience in clinical supply operations, strong knowledge of GxP regulations, cold chain management, and investigational medicinal product (IMP) distribution. The role will collaborate closely with clinical operations, regulatory affairs, and project management teams to ensure smooth execution of global clinical trials.
Professionals seeking clinical research supply chain jobs, clinical trial supply specialist jobs, or biosimilars clinical operations roles should consider applying before the deadline.
Job Overview
Job Title: Clinical Supplies Specialist
Company: Alvotech
Department: Clinical & Medical Affairs (R&D โ iCMR)
Location: Bangalore Office / India Home Office (Partially Remote)
Employment Type: Full Time
Experience Required: 2โ5 Years
Application Deadline: March 15, 2026
The Clinical Supplies Specialist will oversee clinical trial supply planning, procurement, packaging, labeling, distribution, and inventory management for biosimilar clinical studies.
Key Responsibilities
The Clinical Supplies Specialist will be responsible for the following activities:
Clinical Supply Planning
- Develop and maintain clinical supply plans for biosimilar clinical trials
- Integrate patient enrollment forecasts, manufacturing timelines, and protocol requirements
- Conduct risk assessments for supply constraints
Forecasting & Procurement
- Forecast comparator and reference product demand
- Support procurement of reference listed drugs (RLD) and ancillary supplies
- Manage supply strategies aligned with clinical trial timelines
Clinical Supply Operations
- Oversee packaging, labeling, and shipment of investigational medicinal products (IMP)
- Manage cold chain logistics for biologics
- Plan and monitor IMP distribution and returns
Vendor & Budget Management
- Work with vendors for inventory reports and supply chain oversight
- Manage RFPs, SOWs, and vendor contracts
- Track vendor KPIs and service-level agreements
Compliance & Documentation
- Maintain clinical supply documentation in systems such as IRT, ERP, and eTMF
- Ensure compliance with ICH-GCP, GMP, FDA, EMA, and global regulatory requirements
- Support regulatory inspections as clinical supply SME
Cross-Functional Collaboration
- Work with Clinical Operations, Clinical Science, Regulatory Affairs, and Project Management
- Develop supply forecasts based on enrollment and drug usage trends
Qualifications
Education
- Degree in Pharmacy, Life Sciences, Biotechnology, or related field
Experience
- 2โ5 years of experience in clinical supply management
- Experience with biologics or biosimilar clinical trials preferred
Technical Skills
- Knowledge of GxP compliance (GMP/GCP)
- Understanding of cold chain logistics for biologics
- Experience with IRT systems and clinical trial supply forecasting tools
- Familiarity with clinical trial supply chain processes
Additional Skills
- Strong organizational and project management skills
- Ability to work in cross-functional global teams
- Knowledge of biosimilar regulatory requirements
Salary & Benefits
Estimated salary range for this role in India:
โน10 LPA โ โน18 LPA (depending on experience)
Additional benefits may include:
- Hybrid/remote working options
- Global clinical research exposure
- Learning opportunities in biosimilar development programs
- Career growth within biopharmaceutical R&D
About Alvotech
Alvotech is a fully integrated specialty biopharmaceutical company specializing in biosimilar medicines. The company focuses on developing and manufacturing high-quality biologic therapies that improve global patient access.
The Integrated Clinical and Medical Research (iCMR) department drives clinical strategies aligned with global biosimilar regulatory requirements and supports post-marketing authorization activities.
How to Apply
