Manager, Medical Writing

Who We Are
Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with The opportunity A Manager, in Global Regulatory Medical Writing, writes and edits clinical regulatory documents, including submission summaries and other complex documents, provides basic-level oversight and guidance, as well as resource management for the direct medical-writing support in the production of clinical research documentation used in drug development and product registrations How Youll Spend Your Day Primarily works at a project level Writes and edits clinical regulatory documents including study reports, protocols, briefing books, investigators brochures, health authority responses, and other submission documents (e-g, module 25 and modules 27x) Compiles, analyzes, and summarizes data from various sources Conducts proofreading, editing, document formatting, and comment resolution Ensures documents include the proper content and context (from a regulatory medical writing perspective) and clear and consistent medical/scientific messaging, are accurate and complete, and adhere to applicable regulatory guidelines and departmental and editorial standards May participate in the preparation/revision of document templates and SOPs May train and support medical writers or external vendors/contractors on document planning, processes, and content development Your Experience And Qualifications Bachelor's, Master's, MD, PhD, PharmD in life sciences (or other related field) Preferred Master's, MD, PhD, PharmD University degree with a minimum of 5+ years of relevant experience; advanced degree preferred Proficient as lead author writing protocols/protocol amendments, clinical study reports, investigators brochures, and clinical summary documents (modules 25 and 271-274) 6+ years with an advanced degree Travel Requirements: Up to 10% Tevas Equal Employment Opportunity Commitment 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 We are committed to a diverse and inclusive workplace for all If you are contacted for a job opportunity, 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 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