Senior Medical Writer Vacancy @ Novo Nordisk – Apply Online
Novo Nordisk Senior Medical Writer vacancy, Pharmacy job opening 2023, M Pharma job opening 2023, Pharmacy job opening 2023, Novo Nordisk job opening 2023, Pharma job opening 2023, Pharmacy job opening. Intrested and eligible candidates may check out all the details
Job Title: Senior Medical Writer
Location: Bangalore, India
Eligbility Criteria:
You are expected to have the below skills and knowledge:
- Graduate (PhD, MSc., M Pharm, or equivalent).
- 5+ years of experience as 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 from the pharmaceutical /CRO industry.
- Strong understanding of external requirements related to regulatory documents.
- Works independently on smaller tasks.
- Strong analytical skills.
- Committed, persistent and accountable.
- Able to manage variable workload.
- Able to handle numerous tasks simultaneously.
- Prioritizes own tasks but may need to seek advice.
- Requires good communication and analytical skills
The position
The key responsibilities in this position will be to perform medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to preparation of Protocols, Clinical Trial Reports (CTRs), Non-interventional study reports
(NSRs), Layperson Summary (LPS), Investigator Brochure (IB), Regulatory response documents (Q&A), Clinical summaries and Clinical overviews. The tasks, to a large extent, will have to be performed independently. You will have to communicate the clinical data in a clear and concise manner.- Ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally.
- You will contribute to process improvements, knowledge sharing, skill building, and mentor and train other medical writers as needed. You will have to maintain good relationship with the stakeholders and colleagues.
- Responsible in order to meet timelines, the medical writer must be good at planning own work and be proactive when problems arise and seek help and advice from relevant people within GBS as well as within HQ.
- You will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved.
- Frequent travelling abroad to attend meetings in HQ and CMRs, and conference and courses world-wide, will be the part of the job.
Apply Online
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