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Sr Dir IT Global Clinical Operations & Global Program Leadership

$190.08k - $237.6k

Tevapharm

Sr Dir IT Global Clinical Operations & Global Program Leadership Date: Apr 7, 2026 Location: Parsippany, United States, New Jersey, 07054 Job Id: 67083 Our Team, Your Impact The Clinical Operations IT Lead is a strategic and technical leader responsible for driving the digital ecosystem that powers clinical trials research activity. Additionally, this role will be responsible for the IT management for the Global Program Leadership team who provide oversight for the Teva Research & Development Drug Portfolio. This role oversees technology strategy, and emerging AI capabilities to ensure high‑quality, compliant, and efficient study execution. The ideal candidate brings a strong blend of business insight, technology fluency, and value‑driven execution. They leverage deep knowledge of clinical operations to shape technology enhancements that improve execution, maintain a clear view of the vendor and technology landscape, and drive measurable value across the research technology ecosystem—optimizing systems, improving data quality, and ensuring that technology investments deliver meaningful impact for clinical teams and study outcomes. This leader directs a high‑performing team accountable for implementing, maintaining, and optimizing the clinical operations and global program leadership technology ecosystems. The ideal candidate will live within a commutable distance to Parsippany, NJ or West Chester, PA. How You’ll Spend Your Day Strategic Business Partner Works in tight coordination with business teams to align on priorities and develop multi‑year capability roadmaps that drive operational excellence to improve scientific outcomes. Clinical Systems Stewardship Owns the governance of clinical operations and program leadership technologies, translates business needs into technical solutions and system enhancements. Promotes AI/ML solutions Such as predictive modeling, including automated data processing and quality checks. Compliance, Security & Governance Ensures the clinical operations systems comply with regulatory and institutional requirements, including FDA 21 CFR Part 11, GCP, HIPAA, GDPR; develops the long‑term roadmap and oversees budgets, timelines, and performance metrics for technology initiatives. Your Skills and Experience Education: Bachelor’s degree required (Masters/MBA preferred). 15+ years of experience in clinical research IT/informatics or clinical data management (pharma experience preferred). Expertise in core clinical operations systems and data platforms (e.g., CTMS, EDC, eTMF, RTSM). Robust understanding of system validation principles, data integrity, and regulated system expectations. Proven ability to lead cross‑functional teams and complex programs; strong communication skills with the ability to influence stakeholders at all levels. Strategic, innovative mindset to modernize research operations and program leadership using technology, data capabilities, and AI/ML—anticipating trends to improve trial efficiency and data quality. Strong business insight to translate workflow needs into technical solutions; evaluate the technology ecosystem, manage vendors/platform selection, and deliver measurable value through performance and workflow optimization. Salary Range The annual starting salary for this position is between $190,080 – $237,600 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. How We’ll Take Care of You From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), tailored health support, and meaningful ways to give back to the community. Career development is supported through a wide range of learning programs and opportunities for internal growth, empowering you to reach your goals and prioritize your wellbeing. 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. Request a reasonable accommodation by sending an email to View email address on click.appcast.io with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address. Important notice to Employment Agencies - Please Read Carefully Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. #J-18808-Ljbffr Tevapharm

Vacancy posted 4 days ago
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