Safety Surveillance Advisers And Specialists

2+ years

Not Disclosed

Remote

10 Nov. 11, 2024

Job Description

Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Safety Surveillance Advisor/Specialist – Diabetes & Cardiovascular Teams

Location: Søborg, Denmark / Bangalore, India
Department: Global Patient Safety, Novo Nordisk

Are you passionate about patient safety?

Novo Nordisk is looking for Safety Surveillance Advisors and Specialists to join our teams working on high-profile drug development projects. In this dynamic and impactful role, you will play a crucial part in ensuring the highest safety standards and minimizing risks for patients using Novo Nordisk products in diabetes and cardiovascular treatments. If you're eager to make a difference in the safety landscape of the pharmaceutical industry, this is your opportunity to be at the forefront of drug safety.

The Position

As a Safety Surveillance Advisor/Specialist, you will be responsible for the comprehensive safety surveillance of products at various stages of development (clinical trials) and those already in the market. You will utilize your clinical expertise to assess safety data, contribute to developing the safety profile of Novo Nordisk's drugs, and play an essential role in risk management and decision-making processes.

Your key responsibilities include:

Safety Data Evaluation: Collect, analyze, and assess safety data to ensure optimal product safety profiles, both in clinical development (Phase II and III) and post-marketing.
Benefit-Risk Assessment: Contribute to critical risk-benefit analyses and communicate the outcomes to stakeholders across departments.
Cross-functional Collaboration: Represent the Safety Surveillance team in cross-functional project teams and provide medical expertise for ongoing and new drug development.
Leadership: Potentially chair the Novo Nordisk Safety Committee and guide safety-related decisions across multiple teams.
Global Insights: Work closely with Clinical Development, Regulatory Affairs, and other functional teams, gaining insights across the full lifecycle of Novo Nordisk products.

This role offers the opportunity to work independently, while also being a valued member of a collaborative team. You will contribute directly to safeguarding patient health and will work across a range of global markets and therapeutic areas.

Qualifications

To succeed in this role, we are looking for candidates who have:

A Master’s degree in Life Sciences (e.g., Pharmacy, Medicine, Veterinary Science, Biological Sciences). A PhD is preferred.
Several years of experience in drug safety, pharmacovigilance, or drug development. Experience in clinical trials will be an advantage.
A strong understanding of medical concepts, disease processes, scientific methodology, and data analysis.
Excellent IT skills, with proficiency in Microsoft Office and knowledge of industry-standard systems.
Strong written and spoken English communication skills.
An ethical compass and a passion for ensuring patient safety.

Additionally, your proactive mindset, problem-solving skills, and teamwork spirit will be essential in this collaborative, multicultural environment.

About the Department

Safety Surveillance is a vital part of Global Patient Safety, overseeing all safety information for Novo Nordisk products in both development and marketed stages. Based in Søborg, Denmark and Bangalore, India, our team ensures that safety data is carefully monitored, assessed, and communicated across various global teams. We are dedicated to creating a positive and inclusive work atmosphere, and we invite you to be part of our mission to safeguard patients and drive innovation.

Working at Novo Nordisk

At Novo Nordisk, we do not wait for change – we drive it. We are a dynamic company in a rapidly evolving industry, with a focus on innovation and excellence. Our culture fosters a spirit of experimentation and encourages employees to take ownership and seize development opportunities. From research and development to manufacturing and sales, we all work together to improve patient care and drive meaningful change in the healthcare landscape.

How to Apply

If you are ready to make an impact in the field of drug safety and join a high-performance team, apply now. To ensure an efficient and fair recruitment process, please submit your CV without including a photo. You can also briefly explain why you are interested in the role directly in your resume or CV – no cover letter is required.

Deadline

The application deadline is 11 November 2024, but applications will be reviewed on an ongoing basis. We encourage you to apply as soon as possible.

Equal Opportunity Employer

At Novo Nordisk, we are committed to creating an inclusive culture that celebrates the diversity of our employees and the patients we serve. We strive to create a workplace where diverse perspectives, backgrounds, and cultures are valued and contribute to better outcomes for all. We are an equal opportunity employer and encourage individuals from all walks of life to apply.

Contact

For further information, please reach out to:

Lenea Nørskov Blanc at +45 3075 4514
Joakim Isendahl at +45 3075 8235

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Safety Surveillance Advisers And Specialists

Job Description

Job Title: Safety Surveillance Advisor/Specialist – Diabetes & Cardiovascular Teams

Are you passionate about patient safety?

The Position

Qualifications

About the Department

Working at Novo Nordisk

How to Apply

Deadline

Equal Opportunity Employer

Contact

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