Associate Director, R&D Project Management - Innovative Medicines - TevaPharm : Job Details

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 We are seeking a seasoned Associate Director, R&D Project Management to lead the global development of our R&D Innovative Medicine products.In this role, you will be responsible for delivering a product development strategy working in close partnership with a Senior Program Leader to establish, maintain and deliver the priority product plan for both early and late stage.How you'll spend your day Manage Cross-Functional Teams: Drive the operational planning and delivery of development programs, ensuring timely and budget-conscious execution.Innovate and Collaborate: Work closely with global project leaders and function leads to secure approvals, manage risks, and ensure resource allocation.Manage Multiple Projects: Oversee a selection of projects, ensuring all documentation is accurate and up-to-date.Lead quality risk management: Ensure significant risks to the programs have planned mitigations and are flagged in terms of likelihood and impact, to the relevant leadership.Your experience and qualifications Master's degree in a life scientific field; Advanced scientific degree (M.D., D.O., Ph.D.) - preferredMinimum of 7 years in the innovative pharmaceutical industry with a proven track record in project managementIn-depth knowledge and understanding of innovative drug development, industry guidelines, and regulatory and submissions processes globallyStrong oral presentation skills and advanced experience leading cross-functional project teams – preferredProficiency in Planisware, Microsoft Project, SharePoint, PowerPoint, Word, Excel, and OutlookThis role is based in West Chester, PA – preferred or Parsippany, NJ with a requirement to be onsite three days a week. Willingness to travel domestically and internationally is essential.Enjoy a more rewarding choice We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.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.#J-18808-Ljbffr