Department: Global Medical Affairs GBS Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready
Job Responsibilities Preparing product presentations for field staff and presentations for CMEs for KOLs. Handling product related queries from KOLs. Preparing medical content for various promotional materials including but not limited to visual aids, leave behind leaflets,
Job Title: Manager -Medical Affairs Department: Medical Affairs Location: Kandivali (West), Mumbai Qualification & Experience: · MD Pharmacology with 1year experience in medico-marketing. Key Responsibilities: · Scientific support for New Product launches and established brands · Train medical representatives · Handling
As the Head of Medical Affairs, will be responsible for leading and overseeing all medical affairs activities within Venus Remedies Limited. Reporting directly to the Chief Executive Officer (CEO), play a pivotal role in shaping and executing the medical strategy to
• Experience to prepare and review the documentation required for the ISO 9001:2015, EN ISO 13485, Quality management System, MDR for Medical Devices. • Knowledge and preparing documents such as Quality Manual, Site Master File, SOP’s, Change
Department – GBS , Commercial & Corporate Affairs (CSCA) Do you want to work for an organization that has a strong purpose towards driving change to defeat diabetes and serious chronic diseases such as NASH and Cardiovascular,
Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries
Summary Of Position: Regulatory Affairs Analyst is responsible for providing support in ensuring compliance with EU, US, and global medical device regulatory requirements. This position is primarily focused on supporting international registration requirements triggered by the EU Medical Device
Job Title: Regulatory Manager About Job: The Regulatory Manager is a management role that manages the regulatory activities involved in the India/Srilanka/Nepal/Maldives market. Manage the regulatory compliance and data needs including regulatory quality compliance, regulatory database
Department: RA CMC & Device Are you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready
Department: RA CMC & Device Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in
Department: Global Medical Affairs Can you drive the global strategy for culture, engagement and performance Management at Novo Nordisk? Do you have the interpersonal Skills to navigate in a complex stakeholder landscape and Are you able to motivate,
About our client: Our client brings together Pharmacovigilance expertise, Third party system knowledge and Deep technology to develop well-defined solutions, which address challenges across Medical Affairs, Regulatory and Safety functions. Our client solutions free up responsible personnel within
Business Overview J&J MedTech India (JJMI) J&J MedTech India (JJMI) is the market leader in the Medical Technology industry in India. It is in the business of caring and providing solutions to doctors, patients, and nurses. It
XXX Department - Medical Affairs & Medical Education Location – Mumbai, Delhi, Bengaluru, Chennai, Hyderabad, Kolkata Would you enjoy helping to move the pharmaceutical industry forward by facilitating the generation and communication of scientific data and the sharing of
Department – Commercial GBS Do you want to work for an organization that has a strong purpose towards driving change to defeat diabetes and serious chronic diseases such as obesity, rare blood & rare endocrine diseases?
Department – Commercial GBS Do you want to work for an organization that has a strong purpose towards driving change to defeat diabetes and serious chronic diseases such as obesity, rare blood & rare endocrine diseases?
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries
1. Engage client data management during start up. • Create protocol folder(s) for study documentation. • Add entries into individual protocol spreadsheet. • Review Statement of Work (SOW) for study scope. • Ensure start-up packet delivery