What are the responsibilities and job description for the Clinical Packaging Specialist position at Teva Pharmaceuticals?
The opportunity
Position Summary : A Clinical Packaging Specialist has an understanding and application of principles, concepts, practices, and standards in area of clinical supply logistics. Understands the working knowledge of how clinical research fits into overall R&D. Provides answers for complex issues in area of clinical supply aligned with study plans / protocol. Suggestions are developed that provide solutions to moderately complex problems, which require the regular use of ingenuity and innovation. With limited supervision exercises independent judgment in developing work processes, techniques, and evaluation criteria for obtaining results. Work efforts are reviewed to ensure acceptance by proposed goals. Adjusts to the changing priorities. Ensures that the ever-changing demands have appropriate resource allocation. Acts according to Standard Operating Procedures, Best Practice Guidelines. Takes direction from leader in the clinical supply logistics arena.
Essential Duties & Responsibilities :
The Clinical Supply Generalist essential duties & responsibilities for Generic, Biosimialar and Innovative Studies are listed below :
- Pick and package orders received via IRT systems or manual orders to ensure continuous supply of clinical trial material for all ongoing clinical studies.
- Ship Clinical Trial Material to Clinical Sites and Depots.
- Assist with creation and execution of Master Batch Records.
- Assist with Inventory Control of products using a validated inventory system to ensure clinical available drug supply to support clinical studies.
- Assist with the Inspection and accountability of returns for all supplies. Identify issues.
- Assist with labelling and packaging activities.
- Familiar with import-export of products worldwide.
- Support process generation of department procedures.
- Ability to multi-task and handle multiple projects at once while balancing timelines and priorities across Generics, Innovative Medicines and Biosimiliar Clinical Studies.
Your experience and qualifications
Education Required : High School diploma required. Bachelors preferred.
Experience Required : Minimum of0-1 years’ Experience with Clinical Supply Management : Clinical Trial Packaging / Labeling and / or Distribution and operating in a GMP / highly regulated environment.
Specialized or Technical Knowledge, Licenses, Certifications preferred :
Enjoy a more rewarding choice
We offer a competitive benefits package, including :
