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!
Essential Duties & Responsibilities:
Oversees/Mentors for all document types
Provides leadership/strategy at the therapeutic area level
Contributes substantively in meetings at the therapeutic area level
Leads/Recommends the preparation/revision of document templates, development of process, and preparation/revision of SOPs and guidance documents
Guides medical writing (and other) staff (including senior-level staff) on the organization and presentation of information within documents, as well as the design and format of data displays.
Participates in Clinical Research Organization (CRO) alliance and other outsourcing activities
Provides contractor oversight
Analyzes resource needs and assignments strategically
Performs quality assurance review of documents
Exhibits expert collaboration, conflict-resolution, and influencing skills.
Participates in the recruiting/hiring process, and development of direct reports including identifying learning/training opportunities and executing development plans
Responsible for tracking/proving metrics and established key performance indicators, contributing to the budget process, and handling invoices
Identifies processes that require improvement, and demonstrates "big picture" perspective, leveraging experience, to recommend strategies and solutions
Contributes to manuscript preparation as needed
Experience Required: 10+ years in the pharmacuetical field.
Experience Preferred: 15+ years
Mastery of Microsoft (MS) Word, excellent English, both written and spoken
Considered a proficient manager with significant regulatory medical writing expertise.
Considered an internal expert in all aspects of regulatory medical writing and clinical drug development
Ability to organize and present information and to communicate regulatory medical writing processes and technical and editorial standards
Excellent organizational/planning and problem-solving skills at the therapeutic area level
Works successfully with no direct supervision, and has knowledge of global regulations and guidelines for document submissions
Research & Development
Clinical Development Medical Writing
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Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.
Nearest Major Market: Philadelphia
Teva Pharmaceutical Industries