Emcure Pharmaceuticals Released Job Openings On 20/12/2022.Our company was incorporated as Emcure Pharmaceuticals Private Limited on April 16, 1981 as a private limited companies Act, 1956. Our name embodies our purpose and core belief of the entire company which is to make Effective Medicine to Cure patients for enabling them to lead healthier lives.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Collabera s Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Emcure Pharmaceuticals Recruiting M.Pharma/MS/MD with 10-15Years Experience for For Regulatory Writer position.Complete Details for the Regulatory Writer follows.
Important Details :
- Location :Pune
- No of Vacancies:01
- Details of Salary:₹ 15,00,000 – 16,00,000 P.A.
- Opening date for online Application: 20/12/2022
- Mode of application :Online
Job Description/Skills Required
Medical writers are the unifiers between scientific medical knowledge and written communication for various institutions including hospitals, academic medical centers, or pharmaceutical companies. They often follow one of two paths: scientific medical writing or non-scientific or marketing medical writing. Medical writers translate drug trials and medical study findings as well as clinical data to put into presentations to regulatory documents and for medical journal abstracts that are distributed to a professional audience. Medical writers focus on writing the advertising copy, news releases, and educational materials for general audiences. They work alongside doctors, scientists, and other relevant health professionals to develop their content and create information that is distributed to patients including leaflets or pamphlets or websites and educational materials which include slides and posters. Medical writers need a minimum bachelor’s degree or master’s degree in journalism or English and experience in health and science writing as well as fluency about regulation and approval within the medical field. Development and review of of regulatory documents for DCGI Submissions: Rationale, Prescribing information, label, ABPI etc Preparation of documents for SEC meetings Coordination with PV Team for ADR processing