Location: Bangalore, Karnataka, IN

• Ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally.
• You will contribute to process improvements, knowledge sharing, and skill building, and mentor and train other medical writers as needed. You will have to maintain good relationships with the stakeholders and colleagues.
• Responsible for meeting timelines, the medical writer must be good at planning their work be proactive when problems arise, and seek help and advice from relevant people
• You will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved.
• Frequent traveling abroad to attend meetings in HQ and CMRs, and conferences and courses worldwide, will be part of the job.

Qualification

You are expected to have the following skills and knowledge:

• Graduate (PhD, MSc., M Pharm, or equivalent).
• 5+ years of experience as a medical writer or other relevant work experience.
• Experience in CSR, protocol, IB, informed consent, and clinical summaries and clinical overviews.
• Experience working within a global setting.
• Experience in the pharmaceutical /CRO industry.
• Strong understanding of external requirements related to regulatory documents.
• Strong analytical skills. , committed, persistent, and accountable.
• Able to manage variable workload and able to handle numerous tasks simultaneously.

Apply here: https://careers.novonordisk.com/job/Bangalore-Senior-medical-writer-Karn/1011080801/