Novo Nordisk require Medical Writer | Ph.D, M.Sc, M.Pharm

Pharma Admission

igmpi

pharma admission

igmpi

 

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. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

Post : Medical Writer

About the department 
The Medical Writing unit has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community in a short span of 6-7 years, since its inception in 2011. It is a dynamic mix of young, enthusiastic, qualified and skilled Medical Writers and Publishers who are full of commitment, passion, skills and talent. The team is a right blend of professionals with Masters/PhD in pharmacology, medicine, toxicology etc. with broad background knowledge on different therapeutic areas and medical basics. The team has an average experience of 7-8 years in writing and reviewing regulatory documents and publications.

The position
Your key responsibilities will be to perform clinical trial disclosure medical writing tasks  including but not limited to, preparation, peer quality check and review protocol registration and results disclosure of clinical trials to different registries, lay summaries of clinical trials and other clinical trial disclosure and transparency related deliverables and ensure its timely submission. You will also contribute to knowledge sharing, skill building and good collaboration with stakeholders and colleagues and contribute to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge.

Candidate Profile
• Graduate (PhD, MSc, M.Pharm, MD, DDS, DVM or equivalent)
• ≥2 years of experience with clinical trial disclosure activities
• Experience in scientific research methodology, including designing and conducting experiments, and analysing and reporting experimental results
• Experience with scientific writing in English (publications for peer reviewed journals or equivalent)
• Experience from the pharmaceutical /CRO industry
• Solid experience with drug application processes to FDA and EMEA

Additional Information
Experience : 2+ years
Qualification : PhD, MSc, M.Pharm, MD, DDS, DVM
Location : Karnataka - Bangalore
Industry Type : Pharma/ Healthcare
Functional Area : Clinical Development & Medical - Clinical Research
End Date : 25th January, 2019

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