Teva Clinical Packaging Specialist 

United States, Utah, Salt Lake City 

162252938

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.

High School diploma required. Bachelors preferred.
Minimum of 0-1 years’ Experience with Clinical Supply Management: Clinical Trial Packaging / Labeling and/or Distribution and operating in a GMP/highly regulated environment.
• Ability to work under tight deadline and fast-paced undefined environment.
• Have strong organizational skills.
• Ability to work autonomously and/or with a team.
• Excellent problem solving, judgment and decision-making skills.
• Strong verbal, written and presentation skills.
• Superior time management, planning, and organizational skills
• Ability to multitask and effectively prioritize workload.
• Strong client relationship management skills
• Experience with: MS Excel, MS Word, MS PowerPointSpecialized or Technical Knowledge, Licenses, Certifications preferred:

• GMP and/or GCP knowledge and working knowledge of the drug development process and clinical trials.
• Import/export knowledge desirable
• Knowledge of IRT systems

We offer a competitive benefits package, including:
• Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
• Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
• Time Off: Paid Time Off including vacation, sick/safe time, caretaker time, 13 paid Holidays and 3 paid floating holidays.
• Life and Disability Protection: Company paid Life and Disability insurance.
• Additional benefits include, but not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.

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