Are you looking to advance your career in the pharmaceutical industry? Novo Nordisk, a global healthcare leader, is hiring for 4 key roles in Bangalore, Karnataka. If you have a passion for pharmacovigilance, clinical development, or medical affairs, this is your chance to join a company that is making a difference in millions of lives worldwide. Read on to learn more about these opportunities and how to apply.
1. Safety Operations Specialist I
Category: Reg Affairs & Safety Pharmacovigilance
Location: Bangalore, Karnataka
Job Description:
As a Safety Operations Specialist I, you will play a critical role in ensuring the safety of medicinal products. Your responsibilities will include:
- Handling adverse events and safety information to meet global regulatory requirements.
- Leading projects across functional areas, defining scope, goals, and deliverables.
- Managing deviations and change requests, facilitating root cause investigations, and driving corrective actions.
- Collaborating with affiliates to implement new processes based on regulatory demands.
Qualifications:
- Graduation/post-graduation in life sciences.
- Minimum 6 years of pharmacovigilance experience.
- Strong knowledge of GxP requirements and pharmacovigilance principles.
- Fluency in English (written and spoken).
Deadline: 14th March 2025
2. Medical Writer
Category: Clinical Development
Location: Bangalore, Karnataka
Job Description:
As a Medical Writer, you will:
- Prepare regulatory documents such as Protocols, Clinical Trial Reports (CTRs), and Investigator Brochures (IB).
- Communicate clinical data clearly and concisely.
- Collaborate with global stakeholders and contribute to knowledge sharing.
Qualifications:
- Graduate (PhD, MSc, M Pharm, or equivalent).
- 2+ years of medical writing experience.
- Strong understanding of regulatory requirements.
- Excellent communication and analytical skills.
Deadline: 28th March 2025
3. Medical Writing Specialist
Category: Clinical Development
Location: Bangalore, Karnataka
Job Description:
The Medical Writing Specialist will:
- Lead high-complexity medical writing tasks and act as a project manager.
- Develop regulatory documents such as Clinical Summaries, Clinical Overviews, and Meeting Packages.
- Mentor and train other medical writers and contribute to process improvements.
Qualifications:
- Graduate (PhD, MSc, M Pharm, or equivalent).
- 10+ years of medical writing experience.
- Expertise in regulatory medical writing and clinical development processes.
- Strong leadership and communication skills.
Deadline: 28th March 2025
4. Global Medical Advisor
Category: Medical Affairs
Location: Bangalore, Karnataka
Job Description:
As a Global Medical Advisor, you will:
- Provide strategic and medical guidance for Novo Nordisk’s product portfolio.
- Engage with Key Opinion Leaders (KOLs) and develop scientific communication strategies.
- Support global medical affairs initiatives and contribute to medical education.
Qualifications:
- M.D. with clinical/research expertise in areas like Endocrinology or Cardiology.
- 2+ years of clinical or pharmaceutical industry experience.
- Strong understanding of drug development and regulatory processes.
- Fluency in English (written and spoken).
Deadline: 5th March 2025
About Novo Nordisk
Novo Nordisk is a global healthcare leader with a 100-year legacy of driving change to defeat serious chronic diseases. With a strong focus on diabetes, obesity, and rare diseases, the company impacts over 40 million patient lives daily. Novo Nordisk is recognized as one of the top 20 most valuable companies globally by market cap.
The company’s success is built on the collaboration of over 63,000 employees worldwide, who bring unique skills and perspectives to the table. Novo Nordisk fosters a culture of innovation, inclusivity, and continuous improvement, making it an ideal workplace for professionals seeking to make a meaningful impact.
Application Link For Safety Operations Specialist I
Application Link For Medical Writer
