Document Controller in Global Development @ Novo Nordisk, Bachelor’s
degree in Pharmacy/Life Science
Category: Clinical Development and Medical
Location: Bangalore, Karnataka, IN
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 15 December 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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