Job Description

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Associate Safety Operations Adviser

Category: Clinical Development and Medical

Location:

Bangalore, Karnataka, IN

Job Title: Associate Safety Operations Adviser.

Are you a proven leader who can set direction and drive team performance? Do you have expertise in driving medical affairs strategy and tactics across therapeutic areas with a focus on diabetes, obesity and cardiometabolic portfolio? Then we might have the right position for you. We are looking for an Safety Operations Advisor who is excited about joining a growing team, working in an international environment. Apply now!

About the department

Global Safety Bangalore has global responsibility for surveillance of Safety and Quality of Novo Nordisk clinical development and marketed products and is responsible for global handling and reporting of adverse event reports.

The position

All tasks in Safety Operations Advisors department demand a large professional insight, self-dependence and competence in making decisions, as well as flexibility, a good comprehensive view and a many-functioned, often international, co-operation.

• Ensure appropriate medical interpretation and evaluation of adverse events reported from world-wide sources, from marketed use.
• Ensure the fulfilment of global regulatory requirements to the collection, evaluation and reporting of safety information on Novo Nordisk (NN) pharmaceutical products i.e., spontaneously reported adverse events, serious adverse events (SAEs) from clinical trials, investigator sponsored trials, named patient supplies and third party trials.
• Maintain a network of safety contacts within HQ and affiliates.
• To be responsible for immediate reporting to the relevant authorities of serious adverse events that may be associated with Novo Nordisk\'s products. Omission or a delay to do so can result in serious consequences for Novo Nordisk.
• To be responsible for the medical evaluation of reports concerning serious adverse events, as well as for the evaluation of possible causal relationships.

Qualifications

• Should Possess Medical Degree (MBBS) / Postgraduate Medical Degree (MD).
• 2+ years in Documented scientific experience, preferably from the pharmaceutical industry.
• Good knowledge of diseases, their clinical manifestations, treatment and complications.
• Good knowledge of clinical pharmacology.
• Good knowledge of computers and databases.
• Fluent English, both written and spoken.

Working at Novo Nordisk

At Novo Nordisk, we have been changing diabetes since 1923. If you are ready to strengthen our position as an innovative pioneer and respected industry leader, we encourage you to join us to make the most of your talent. In exchange, we offer you the opportunity to work with extraordinary talent globally and benefit from a range of possibilities for professional and personal development.

Contact

To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions).

Deadline

21st August,2023.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we\'re life changing.

Novo Nordisk