Novo Nordisk is a renowned global healthcare company with a strong legacy in diabetes care, haemophilia management, growth hormone therapy, and hormone replacement therapy. With a commitment to improving patient outcomes, Novo Nordisk continues to innovate and lead in the pharmaceutical industry.
Job Title: Medical Writer
Job Description
As a Medical Writer at Novo Nordisk, you will play a critical role in ensuring clear, timely, and effective communication across global teams. Your responsibilities will include:
- Preparing high-quality clinical documents such as Protocols, Clinical Trial Reports (CTRs), Non-interventional Study Reports (NSRs), Layperson Summaries (LPS), Investigator Brochures (IB), and Regulatory Response Documents (Q&A).
- Communicating clinical data in a concise and accurate manner.
- Collaborating with stakeholders and colleagues across different time zones and professional environments.
- Planning and managing your workload to meet tight deadlines.
- Providing constructive feedback to expert contributors to improve the quality of clinical documents.
- Contributing to knowledge sharing and maintaining strong relationships with stakeholders.
Candidate Profile
To be considered for this role, you should meet the following criteria:
- Educational Qualification: Ph.D, M.Pharm, Pharm.D, MSc., or equivalent.
- Experience: Minimum of 2+ years as a Medical Writer or in a relevant role within the pharmaceutical or CRO industry.
- Skills:
- Strong understanding of regulatory requirements for clinical documents.
- Excellent communication and analytical skills.
- Ability to work independently and manage variable workloads.
- Proactive problem-solving and planning abilities.
- Attributes: Committed, persistent, and accountable.
Key Responsibilities
- Perform medical writing tasks for trial and non-trial activities.
- Ensure compliance with global regulatory standards.
- Collaborate with global teams to deliver high-quality clinical documents.
- Contribute to continuous improvement in medical writing processes.
Additional Information
- Experience: 2+ years in medical writing or a related field.
- Qualification: Ph.D, M.Pharm, Pharm.D, MSc., or equivalent.
- Location: Bangalore, Karnataka.
- Industry Type: Pharma / Healthcare / Clinical Research.
- Category: Clinical Development.
- Application End Date: 30th March 2025.
