Document Specialist in Global Development , Bachelor’s
degree in Pharmacy/Life Science.
- Clinical Development & Medical
- Bangalore
We are looking for a Document Specialist for medical writing team
in the Global Development (GD) unit based out of Global Service Centre (GSC),
Bangalore, India. You can look forward to an exciting job driving different
projects and engaging with multiple stakeholders at the global level.
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
The main job task in this role is to distribute safety reports and
Investigator’s Brochure (IB) to Novo Nordisk clinical trial sites globally
through CONNECT- Novo Nordisk Investigator Portal. In this role you will
participate in knowledge sharing and skill building activities to maintain good
collaboration with stakeholders and ensure active participation in relevant
meetings, training sessions and seminars in the department locally/globally.
The role is based in GD GSC, Bangalore, India but travel may be
required locally or to Novo Nordisk offices in Denmark or affiliate offices for
business related meetings/conferences. The role doesn’t have a direct influence
on any of the internal or external stakeholders. The ability to work in a global
context is important, as well as cultural awareness and inclusive approach.
Qualifications
You are expected to have the below skills and knowledge.
- Bachelor’s degree in Pharmacy/Life Science (4-year course)
- Minimum 6 months of relevant experience in web based Document Management Systems, MS Office and Portable Document Format (PDF) tools
- General knowledge and understanding of FDA, EMA, ICH GCP and other regulatory electronic documentation requirements for safety reporting
- Ability to communicate, plan and coordinate multiple simultaneous activities
- Fluent in English language (read, write and speak)
- Team player with a high degree of flexibility
- Ability to multitask and prioritise activities
- Demonstrate Novo Nordisk leadership competencies
- Good communication and stakeholder management skills
Working at Novo Nordisk
At Novo Nordisk, we have been changing diabetes since 1923. If you
are ready to strengthen our position as an innovative pioneer and respected
industry leader, we encourage you to join us to make the most of your talent.
In exchange, we offer you the opportunity to work with extraordinary talent
globally and benefit from a range of possibilities for professional and
personal development.
Contact
For further information, please contact Ganesh Shetty at
gsy@novonordisk.com
Deadline
30 September 2019.
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to
change lives for the better for millions of patients living with diabetes and
other chronical diseases. In exchange, we offer the chance to be part of a
truly global workplace, where passion and engagement are met with opportunities
for professional and personal development.
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