[New Job Vacancy] Medical Writing Associate III job in Teva Pharmaceuticals, (Navi Mumbai, Maharashtra) – Jobs in Navi Mumbai, Maharashtra

Are you searching for a Perfect job or looking for new opportunity then this site is the best choice for you to search your dream Job. Job Opening details:- Company Name :- Teva Pharmaceuticals Position Name :- Medical Writing Associate III Company Location :- Navi Mumbai, Maharashtra Job Category :  General Category Full Job Description :- Company Info 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! Job Description BA/BE, Phase 1, FIH, SAD and MAD Generics & Specialty study projects. Literature search, preparation of Clinical study protocols / Specialty protocols(PK/PD) studies, according to Guidelines and Regulatory Requirements by using Product Monographs/Prescribing Information/Summary of Product Characteristics etc., as applicable Preparation of Informed Consent Form/s (ICF) in line with Clinical study protocol MedDRA and WHO-DD coding of clinical studies Specialty brand studies support including medical writing eTMF Management, Periodic Project Update & Hosting project meetings & teleconferences Literature search, preparation of Clinical study protocols and PSP according to required on day to day Guidelines and Regulatory Requirements by using Product Monographs/Prescribing Information/Summary of Product Characteristics etc., as applicable. Preparation of Informed Consent Form/s (ICF) in line with Clinical study protocol. MedDRA and WHO-DD coding of clinical studies Preparation/review of Case Record Forms (CRF). System improvements as basis. Preparation of Clinical Study Reports Qualifications Qualification- MPharm(Pharmacology) Atleast 8 years experience Function Research & Development Sub Function Clinical Development Medical Writing Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on “Employee Central”. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s 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. Disclaimer : We are only helping our audience to check various job listing in various companies. We have not providing any job nor taking any registration fees. We have no legal responsibility over the details mentioned on our website. candidates are requested to check company profile before joining.

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