Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions •
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.
Work Flexibility: Hybrid Who we want: - Detail-oriented process improvers. Critical thinkers who naturally see opportunities to develop and optimize work processes – finding ways to simplify, standardize and automate. - Business-oriented evaluators. People who effectively
The Procurement Excellence team is responsible for: Establish and develop a cost efficient, agile, and high quality supplier base in the region. Strategize the right level of local content, considering regulatory needs, FX exposure, risk management, time-to-market
Are you passionate about market access and health economics? Do you want to make a difference in the healthcare industry? We are looking for a Market Access Sr. Analyst to join our team. If you are
Bidding Manager & Sales Support Brazil M/F (28941) At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose. We are a global leader in medical imaging, offering an
How will you CONTRIBUTE and GROW? The Industrial Pharmacist and Regulatory Manager will be responsible for leading and managing the coordination and management of the product registration process for South Africa and all export territories. The selected
Are you detail-oriented and passionate about ensuring regulatory compliance? Do you have experience in compiling and submitting regulatory documents? We are looking for a Regulatory Affairs Analyst to join our team in the Regulatory Affairs department at Novo Nordisk. If
Job Description Job Description Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy. Provides, under