Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas. We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!
Senior Director (Respiratory) is responsible for the development, execution and management of several clinical programs worldwide across all phases of clinical research. The Senior Director will oversee study teams and will be responsible for leading cross-functional teams in a matrix environment. The individual is expected to be able to function independently in the daily management of clinical research projects including the preparation/review of related key documents (i.e. protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Senior Director is responsible for designing and implementation of the clinical development plan and will provide leadership for assigned asset strategy, working closely with other functional areas such as commercial, regulatory, pharmacovigilance, CMC, and pre-clinical development in this regard. The Senior Director will be a key contributor to and responsible for the clinical leadership of INDs, NDAs, BLAs, and other global regulatory filings. The Senior Director will foster relationships with opinion leaders in assigned disease areas.
Essential Duties & Responsibilities:
Will be a core member of the Global Project Team
Will have and maintain the expertise necessary for the clinical development of the product
Prepares and manages multiple Clinical Development Plans
Leads or oversees the cross-functional clinical development team
Supports Global Clinical Operations in clinical trial initiation, resource planning, study implementation and successful completion
Leads a team of clinical study physicians also accountable for their respective clinical trials.
Pharmaceutical industry experience with 8+ years of experience developing and directing clinical trials.
Require 2-4 years managerial experience.
Board certification and/or strong experience in clinical development in designated therapeutic area(s) strongly
Board certification and medical training
Must speak fluid English and be a proficient scientific writer.
Proven track record of leading studies from early stage through to regulatory submissions.
Research & Development
VP Clinical Development Respiratory, Respiratory TA - US
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