Senior Manager Clinical Statistician

2 years

Not Disclosed

Parsippany

10 Nov. 20, 2024

Job Description

Job Type: Full Time Education: PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Who We Are

At Teva Pharmaceuticals, we are dedicated to making good health more affordable and accessible for millions worldwide. Our mission unites our team across nearly 60 countries, embracing a rich diversity of nationalities and backgrounds.

As the leading manufacturer of generic medicines and a proud producer of numerous products on the World Health Organization’s Essential Medicines List, our medicines benefit at least 200 million people daily. While this is a significant accomplishment, we continually seek new ways to make a difference and welcome individuals ready to contribute.

The Opportunity

We are looking for a Senior Manager Clinical Statistician to provide expert statistical support for clinical studies and programs within Teva Global R&D. This role involves strategic planning, study design, data analysis, and regulatory interactions, requiring a deep understanding of statistical principles and tools.

The ideal candidate will be a strong individual contributor with demonstrated leadership, creativity, and strategic thinking capabilities, as well as excellent communication skills to thrive in a global environment.

Key Responsibilities

Program and Study-Level Contributions

Provide statistical support at the product/program level.
Manage and deliver assignments with quality and timeliness.
Offer input for budget planning.

Study Design and Analysis

Develop study designs, clinical endpoint assessments, and sample size planning.
Write or oversee the preparation of statistical sections of clinical protocols and analysis plans.
Conduct or supervise statistical analyses for clinical study reports, abstracts, manuscripts, and marketing materials.

Regulatory Interactions

Lead the preparation of analyses and documents for global regulatory submissions, including briefing packages and responses.

Team Leadership and Collaboration

Train and oversee team members or contingent workers, as applicable.
Collaborate with outsourcing partners and manage statistical aspects of outsourced studies.
Proactively identify and address process improvements.

Innovation and Best Practices

Implement innovative clinical trial designs, methodologies, and analysis techniques.
Participate in initiatives to improve the global statistics department's effectiveness.

Your Experience and Qualifications

Education and Experience:

MS with a minimum of 4 years of relevant experience, or PhD with a minimum of 2 years of relevant experience.
Extensive knowledge of statistical principles and experience with SAS, JMP, and/or R programming.

Core Competencies:

Expertise in planning, analysis, and reporting of clinical trials.
Experience in outsourcing models (fully or functional outsourcing).
Strong organizational, problem-solving, and leadership skills.
Knowledge of relevant ICH, FDA, and CHMP guidelines.

Job-Specific Requirements:

Ability to contribute to strategic planning under moderate supervision.
Strong communication skills to ensure actionable and collaborative results.
Capacity to tackle difficult problems and implement innovative solutions.

What We Offer

Comprehensive Benefits:

Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on Day 1.
Retirement Savings: 401(k) with employer match (up to 6%) and a 3.75% annual Defined Contribution.
Paid Time Off: Vacation, sick/safe time, caretaker time, 13 paid holidays, and 3 floating holidays.

Wellness and Protection:

Life & Disability Insurance (company-paid).
Health Savings Account, Lifestyle Spending Account, and Employee Assistance Program.

Additional Perks:

Tuition Assistance and Employee Stock Purchase Plan.
Voluntary benefits like accident, critical illness, and hospital indemnity insurance.

Role Details

Function: Clinical Statistics.
Reports To: Senior Leadership within Global R&D.

Already Working @Teva?

Current employees should apply through the internal career site on Employee Central for priority consideration. For assistance with Employee Central, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is an equal opportunity employer. We prohibit discrimination based on age, race, religion, gender, disability, sexual orientation, veteran status, or other protected statuses.

We are dedicated to creating a diverse and inclusive workplace. If accommodations are required during the recruitment process, please inform us. All accommodation information is treated confidentially to ensure an accessible candidate experience.

Important Notice to Employment Agencies

Teva Pharmaceuticals does not accept unsolicited CVs/resumes from agencies without a valid written agreement. Unsolicited referrals will be deemed property of Teva, and no fees will be paid. Introductions must align with specific agreed-upon positions.

Join Teva and contribute to making a global impact on health.

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