Sr Director, Global Clinical Programming

Tevapharm; Chester (Delaware County); Hybrid; USD 211,000 - 270,000; Full time

Job summary

An established industry player is seeking a Senior Director of Global Clinical Programming to lead a dynamic team in enhancing clinical trial processes. This pivotal role involves guiding programming efforts, managing resources, and ensuring compliance with industry standards. The ideal candidate will have extensive experience in clinical programming and a strong background in statistical analysis. Join a forward-thinking company committed to making healthcare more accessible and affordable, where your leadership will directly impact the success of global clinical projects. With a focus on innovation and collaboration, this position offers the opportunity to shape the future of clinical programming within a supportive environment.

Benefits

Comprehensive Health Insurance

401(k) with Employer Match

Paid Time Off

Life and Disability Protection

Tuition Assistance

Employee Stock Purchase Plan

Flexible Spending Accounts

Health Savings Account

Virtual Physical Therapy

Paid Parental Leave

Qualifications

• 13+ years of experience in pharmaceutical or clinical research as a programmer.
• Strong leadership skills to guide the clinical programming team.

Responsibilities

• Lead and mentor the Clinical Programming team across global projects.
• Ensure compliance with SOPs and industry guidelines.

Skills

SAS Programming

Clinical Programming

Leadership

Project Management

Data Presentation

Education

Bachelor’s Degree in Science

Master’s Degree in Statistics

PhD in Information Technology

Tools

Statistical Software

Project Management Tools

Job description

Sr Director, Global Clinical Programming

Date: Apr 11, 2025

Location: West Chester, United States, Pennsylvania, 00000

Job Id: 61459

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.

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.
• Oversee contingent workers and/or vendors; provide training to others; strategically analyze needs to manage resources and accountable for resource allocation.
• Lead and manage the global clinical programming activities with strong programming skills.
• Initiate and lead multi-disciplinary pivotal projects to improve operational processes related to Clinical Trials execution, Data Presentation and Knowledge Management.
• Leverage the managerial team's professional standards and abilities while preserving a fluent workflow with other interfacing departments.
• Ensure 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 Insurance and Long Term Disability.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

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.