Job Description

Who we are

Together, we\'re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It\'s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world\'s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization\'s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we\'re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

Clinical Supply Manager are responsible for the successful provision of supplies to patients enrolled in clinical trials; this includes communicating and driving timelines both internally and externally, working with stakeholders to ensure the correct drug/other clinical trial supply is in the right place on time for dispensing to patients. This includes management and oversight of the planning, forecasting, distribution and return of clinical supplies.

How you\'ll spend your day

• Designs and executes clinical supply chain strategies with planning and forecasting of supplies in collaboration with stakeholders.
• Interacts with HOD and finance to develop budgets and manage costs for clinical supply activities.
• Oversight, coordination, and collaboration with internal stakeholders / vendors to ensure delivery of IMP and related materials at the right time and quality level.
• Planning, preparing, surveillance and facilitating of IMP and related materials for clinical trials.
• Identify supply accountability tracking and ensure Master, Pharmacy, Subject Logs are appropriate.
• Collaborate with study team and vendors to assure proper distribution of supplies to study sites.
• Manage approval of the packaging and logistics service agreements and study specific plans
• Develops, maintains, and executes an optimal resupply strategy with proactive planning, appropriate lead-time.
• Ensure compliance and continuity of clinical supplies, including proactive expiry management of clinical supplies.
• Critically evaluate the available information and provide advice to create a robust and flexible supply chain strategy that ensures drug availability but also minimizes waste.
• Perform risk assessment at project initiation and assess throughout the project, mitigate any project risks identified.
• Exhibit professional, clear, and timely verbal and written communication skills.
• Lead, organize, and present at meetings, business review meetings.
• Preparing and reviewing SOPs, deviations, complaints and CAPAs
• Responsible for supporting other CTS teams as applicable.
• Manage the personnel\'s actions including, but not limited to performance management, scheduling and work assignments, disciplinary action, promotions etc.

Your experience and qualifications

• Master\'s degree with 10+ years of experience working in a clinical research (clinical operations) environment; 6+ years of direct \xe2\x80\x9chands-on\xe2\x80\x9d in the Clinical trial Supplies/Supply Chain.
• Proven Project Management experience within supply chain environment
• Able to demonstrate sole accountability for project delivery.
• Strong knowledge of Good Distribution Practices, Good Clinical Practice and ICH guidelines, and other applicable regulatory requirements
• Strong ability to manage time and work independently.
• Excellent written and verbal communication skills. Proficient in English language is required
• Ability to establish and meet multiple concurrent priorities and deadlines.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva\'s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva\'s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Teva Pharmaceuticals