Associate Director, Business Strategy and Operations, Global Statistical and Data Sciences

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

The Associate Director of BSO is a business operations lead who collaborates with the GSD Leadership Team to ensure GSD’s long-term operational excellence. Under the guidance of the Head of BSO, this role supports GSD quality and vendor management. The Associate Director is responsible for coordinating GSD Trial Master File (TMF) management and Inspection Readiness preparations. As the GSD quality lead, this role collaborates closely with the GSD functional subject matter experts in GSD Job Aid management and process improvement. Additionally, the Associate Director liaises with R&D Clinical Quality Assurance and Training to track and resolve procedural deviations, as well as ensure training compliance with company policies and procedures. The Associate Director also supports GSD vendor management, including vendor evaluation, contract negotiation, vendor performance assessment, compliance monitoring, and budget management.

Travel Requirements:  International or Domestic

 

The ideal candidate in this role can be onsite at the West Chester, PA location 3 days a week, however, we are open to considering a remote based employee if qualified

How you’ll spend your day

• Primarily work on the multiple product/program level
• Collaborate with Procurement in vendor evaluation and contract negotiation
• Evaluate vendor performance in quality, timely delivery, and adherence to agreed-upon standards. Track and promptly report issues to GSD management
• Support GSD functional managers in purchase order, accrual, and invoice tracking and issue resolutions
• Coordinate GSD TMF reviews and inspection readiness preparations
• Support GSD job aid creations and maintenance
• Liaise with Processes & Procedures in GSD procedural deviations and quality events tracking and resolution
• Liaise with Training and monitor GSD training compliance
• Support, contribute to, and lead BSO initiatives
• Possibly to have direct reports; Oversees contingent workers and/or vendors; Provides training to others; Strategically analyzes needs to manage resources

Your experience and qualifications

Required:

• Master or PhD in statistics, data science, computer science, life sciences or other related fields with minimum of 6 years of relevant pharmaceutical experience

 

Functional Knowledge:

• Subject matter expert in statistical, programming, and medical writing processes and activities. Knowledge in clinical trials and regulations. Project management skills or prior experience in managing projects related to regulatory activities. Experience working with vendors or CROs on clinical trial related activities.

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. 

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: Internal Career Site

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