
Associate Director, Clinical Trials Materials
Are you a driven and experienced professional in the pharmaceutical industry? Do you have a passion for ensuring the successful execution of clinical trials? IQVIA is seeking a highly qualified and motivated individual to join our team as Associate Director, Clinical Trials Materials. In this role, you will play a crucial role in overseeing the supply and distribution of materials needed for clinical trials, ensuring the timely and efficient delivery of critical supplies to support the advancement of life-saving treatments. If you have a strong background in clinical trials materials management and are looking for a challenging and rewarding career opportunity, we encourage you to apply for this position.
- Manage and oversee all aspects of clinical trial materials, including planning, forecasting, procurement, packaging, labeling, and distribution.
- Collaborate with cross-functional teams to develop and implement supply chain strategies and ensure timely delivery of materials to clinical trial sites.
- Monitor and track inventory levels to ensure adequate supply for ongoing and upcoming trials.
- Conduct regular audits of clinical trial material processes and systems to identify areas for improvement and implement corrective actions.
- Develop and maintain relationships with vendors and suppliers to negotiate favorable pricing and ensure quality and timely delivery of materials.
- Ensure compliance with all relevant regulations, standards, and guidelines related to clinical trial materials management.
- Train and mentor team members on best practices for clinical trial materials management.
- Prepare and manage budgets for clinical trial materials and track expenses to ensure adherence to budgetary constraints.
- Provide regular updates and reports on material supply status to project teams and management.
- Stay informed about new developments and advancements in clinical trial materials management and implement best practices accordingly.
- Identify and proactively address potential supply chain risks and issues to ensure the successful execution of clinical trials.
Advanced Degree In Pharmacy, Life Sciences, Or Related Field.
Minimum Of 8 Years Of Experience In Clinical Supply Chain Management Or Related Field.
Strong Understanding Of Global Clinical Supply Chain Regulations And Guidelines.
Experience Managing Multiple Clinical Trials And Supply Chain Vendors.
Excellent Project Management And Leadership Skills.
Risk Management
Quality Assurance
Project Management
Procurement
Vendor Management
Logistics
Budget management
Inventory Control
Auditing
Supply Chain
Team Leadership
Regulatory compliance
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
creativity
Attention to detail
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Associate Director, Clinical Trials Materials is $105,000 - $145,000 per year. However, this can vary depending on factors such as location, experience, and the specific company or organization the individual is working for. Some companies may offer higher salaries or additional benefits, such as bonuses and stock options, for this position. It is also possible for individuals to negotiate their salary based on their qualifications and the demand for their skills in
Apply with Video Cover Letter Add a warm greeting to your application and stand out!
IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.

Get interviewed today!
JobzMall is the world‘ s largest video talent marketplace.It‘s ultrafast, fun, and human.
Get Started