
Safety Surveillance Adviser
Welcome to Novo Nordisk, a global healthcare company dedicated to improving the lives of people with chronic diseases. We are currently seeking a highly motivated and experienced individual to join our team as a Safety Surveillance Adviser. This role is crucial in ensuring the safety and efficacy of our products, as well as maintaining compliance with regulatory requirements.As a Safety Surveillance Adviser, you will be responsible for monitoring and evaluating the safety profile of our products, identifying and analyzing potential safety concerns, and collaborating with cross-functional teams to develop risk management strategies. Your expertise and attention to detail will play a critical role in maintaining the high standards of quality and safety that Novo Nordisk is known for.To be successful in this role, you must have a degree in a relevant scientific field, along with at least 3 years of experience in pharmacovigilance or drug safety. Strong analytical skills, excellent communication abilities, and a proactive attitude are also essential for this position. If you are passionate about making a difference in the healthcare industry and have the necessary qualifications, we invite you to apply and become a valuable member of our team.
- Monitor and evaluate the safety profile of Novo Nordisk products.
- Identify and analyze potential safety concerns.
- Collaborate with cross-functional teams to develop risk management strategies.
- Ensure compliance with regulatory requirements related to drug safety.
- Keep up-to-date with new regulations and guidelines related to pharmacovigilance.
- Participate in safety surveillance activities and meetings.
- Conduct literature reviews and signal detection activities.
- Perform data analysis and interpret safety data from clinical trials and post-marketing surveillance.
- Prepare and submit safety reports to regulatory authorities.
- Communicate with healthcare professionals and patients regarding adverse events.
- Provide expert safety advice to internal stakeholders.
- Monitor and assess the effectiveness of risk management plans.
- Participate in the development and review of safety-related documents, such as protocols, investigator brochures, and product labeling.
- Train and educate team members on drug safety processes and procedures.
- Represent the company in external safety-related meetings and conferences.
- Maintain accurate and up-to-date records of safety-related activities.
- Proactively identify areas for improvement in safety surveillance processes and suggest solutions.
- Adhere to ethical and legal standards related to pharmacovigilance.
- Uphold the company's values and promote a culture of safety and patient-centricity.
- Continuously strive to improve the safety and efficacy of Novo Nordisk products, in line with the company's mission.
Bachelor's Degree In A Related Field Such As Pharmacology, Public Health, Or Occupational Health And Safety.
Minimum Of 3 Years Of Experience In Drug Safety Surveillance Or Related Field.
In-Depth Knowledge Of Pharmacovigilance Regulations And Guidelines, Including Ich And Fda Guidelines.
Strong Analytical And Problem-Solving Skills, With The Ability To Interpret Complex Data And Make Risk Assessments.
Excellent Communication And Teamwork Abilities, With The Ability To Collaborate With Cross-Functional Teams And Present Findings To Stakeholders.
Risk Management
Quality Assurance
Data Analysis
Compliance Management
Risk assessment
Medical Writing
Pharmacovigilance
Safety Reporting
Safety Monitoring
Signal Detection
Safety Communication
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Active Listening
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Safety Surveillance Adviser in Bengaluru, Karnataka, India is between ₹500,000 - ₹800,000 per year. This can vary depending on factors such as experience, education, and the specific company or industry.
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Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.

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