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Senior Director Clinical Development - Neurology

2-4 years
Not Disclosed
10 Nov. 21, 2024
Job Description
Job Type: Full Time Education: MD/DO/PhD/Pharm.D/DVM 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 on a mission to make good health more affordable and accessible, helping millions around the world live healthier lives.

  • Operating in nearly 60 countries, we are a diverse organization representing a variety of nationalities and backgrounds.
  • We are the leading manufacturer of generic medicines and producers of many products listed on the World Health Organization’s Essential Medicines List.
  • Every day, 200 million people worldwide rely on our medicines.

We are continually looking for innovative ways to make a difference—and for talented individuals to join us on this mission.


The Opportunity: Senior Director, Clinical Research

Position Overview

The Senior Director, Clinical Research is responsible for managing global clinical programs across all phases of clinical research. This role includes leadership in cross-functional, matrixed environments and development of key clinical documents such as protocols, Investigator’s Brochures, and regulatory submissions.

The Senior Director provides clinical leadership for asset strategies and plays a critical role in INDs, NDAs, BLAs, and other global regulatory filings, collaborating with teams across commercial, regulatory, pharmacovigilance, and pre-clinical functions.


Key Responsibilities

Leadership & Strategy

  • Core member of the Global Project Team.
  • Develops and oversees Clinical Development Plans (CDPs).
  • Leads cross-functional clinical development teams.
  • Provides clinical expertise for product development and strategic direction.

Clinical Trial Management

  • Supports trial initiation, resource planning, implementation, and completion.
  • Ensures compliance with ICH, GCP, and local regulations.
  • Addresses clinical safety concerns with stakeholders as needed.

Regulatory Contributions

  • Oversees preparation of regulatory documents (INDs, NDAs, etc.).
  • May lead NDA submission teams independently.

Collaboration & Communication

  • Builds relationships with opinion leaders and external stakeholders.
  • Represents Teva at scientific meetings, advisory boards, and regulatory meetings.
  • Partners with teams in Regulatory Affairs, Biostatistics, CMC/Formulations, and more.

Scientific Contributions

  • Authors/reviews clinical documents, including protocols, study reports, and publications.
  • Analyzes and interprets clinical trial data.
  • Prepares abstracts, posters, and manuscripts; presents data at scientific forums.

Preferred Qualifications

  • MD, DO, PhD, PharmD, or DVM (MD/DO preferred).
  • Minimum 3 years’ pharmaceutical industry experience (Neurology and rare disease preferred).
  • Proven ability to lead teams and manage multiple priorities.
  • Strong communication, interpersonal, and analytical skills.

Work Environment

  • Location: Hybrid (West Chester, PA or Parsippany, NJ), with remote flexibility for qualified candidates.
  • Travel: Up to 30% domestic and international.

Why Join Us?

We offer a competitive benefits package, including:

  • Health Insurance: Medical, Dental, Vision, and Prescription coverage from Day 1.
  • Retirement Savings: 401(k) with employer match (up to 6%) and 3.75% defined contribution.
  • Paid Time Off: Vacation, sick time, holidays, and floating holidays.
  • Life and Disability Insurance: Company-provided coverage.
  • Additional Benefits: Tuition assistance, Employee Stock Purchase Plan, paid parental leave, flexible spending accounts, and more.

Equal Employment Opportunity

Teva is committed to diversity and inclusion. We provide equal employment opportunities regardless of age, race, gender, disability, or any legally recognized status. Accommodations during the recruitment process are available upon request.

Join us in making a difference in global health.