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Sr Director, Global Clinical Programming

Teva Pharmaceuticals
West Chester, United Statesfull_timeVerifiedPosted 11 Apr 2025
💰 $270,000/yr($211,000/yr$270,000/yr)

About the role

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 clinical programming department provides SAS programming support; develops and generates official outputs and datasets for regulatory purposes.

 

The primary responsibility of the Senior Director, Global Clinical Programming is to lead, mentor, educate and direct all global clinical programming aspects within the R&D division and manage the resources globally. Within this scope of responsibility, the Senior Director is also responsible for planning and providing programming support and submission ready deliverables to clinical drug development projects conducted by the company’s R&D, Marketing, PhV, Medical Affairs and other departments.

 

Location: For candidates local to our Parsippany, NJ or West Chester, PA offices, this will be a hybrid role (3 days/week onsite). However, there is flexibility for the role to be remote for non-local candidates. Relocation assistance may be available for non-local candidates as well.

How you’ll spend your day

  • Provide guidance and vision for leading the Clinical Programming team.
  • Directly accountable for your team budget
  • Will have direct reports; Oversee contingent workers and/or vendors; Provide training to others; Strategically analyze needs to manage resources and accountable for resource allocation
  • Leads and manages the global clinical programming activities. Has strong programming skills.
  • Initiates and leads multi-disciplinary pivotal projects to improve operational processes, related to Clinical Trials execution, Data Presentation and Knowledge Management.
  • Leverages the managerial team's professional standards and abilities, while preserving a fluent workflow with other interfacing departments.
  • Ensures that SOPs and guidelines are followed, and the clinical programming processes are well known by all teams
  • Pro-actively collaborate with other departments and share the knowledge of programming and data presentation skills.
  • Keep abreast of the industry programming and technological advancements.

 

Knowledge and Competencies

This role will require the ability to:

  • lead the creation of technical capabilities that promote cutting-edge programming tools
  • leverage experience with respect to industry guidelines and standards.
  • influence Clinical Programming processes.

Your experience and qualifications

  • Bachelor’s Degree, Master’s Degree, or PhD in Science, Statistics, Information Technology OR equivalent combination of education and related work experience.
  • Bachelor's degree with minimum 13 years of experience, Master's degree with minimum 12 years of experience, or PhD with minimum 10 years of experience in a pharmaceutical or clinical research setting as a programmer.

Compensation Data

The annual starting salary for this position is between $211,000 - $270,000 annually. Factors which may affect starting salary within this range and level of role may include geography/market, skills, education, experience and other qualifications of the successful candidate. 

Enjoy a more rewarding choice

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 and holidays.

· Life and Disability Protection: Company paid Life and Disability insurance.

· Additional benefits include, but are 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 Insu

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Company

Teva Pharmaceuticals

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