Novo Nordisk looking for Associate Medical writer

Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy.

Post : Associate Medical writer

The key responsibilities in this position will be to perform medical writing for trial and/or non-trial activities within clinical reporting including preparation of Clinical Trial Reports (CTRs), clinical trial results presentations for distribution to clinical investigators. Also, you need to perform publication planning task. You will contribute to skill building and suppose to have a good collaboration with the stakeholders and colleagues. You will also contribute to ongoing improvements in cross-functional and global collaboration and sharing of best practices and knowledge. The tasks will, to a large extent, be performed independently in agreement with the immediate superior and Clinical Reporting. The Medical Writer will act as Project Manager for the task in question, and in accordance with project goals, Novo Nordisk SOPs and applicable internal and external requirements.

You should ensure timely, clear and proactive communication and collaboration with the stakeholders and colleagues globally . You will communicate across the time zones and in different professional environments. This job requires good communication and analytical skills. 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 GD GBS as well as within GD, 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.

Candidate Profile :
• Graduate (PhD, MSc., MPharm, or equivalent)
• 2+ years of experience with scientific research methodology, including designing and conducting experiments, and analysing and reporting experimental results
• 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 work load
• Able to handle numerous tasks simultaneously
• Recognizes problems; may need advice to solve
• Prioritizes own tasks but may need to seek advice

Additional Information
Qualification : Graduate (PhD, MSc., M.Pharm, or equivalent)
Experience : 2+ years
Location : Bangalore
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Clinical Development and Medical
End Date : 30th June, 2021