SENIOR MEDICAL WRITER IN GLOBAL DEVELOPMENT, MSC,
M PHARM, MD, DDS, DVM OR EQUIVALENT
We
are looking for a Medical Writer 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 Master’s/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
key responsibilities in this position will be to perform medical writing tasks
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 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.
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. The 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 GSC as well
as within GD, Headquarter.
Qualifications
You
are expected to have the below skills and knowledge.
Post
Graduate (PhD, MSc, M Pharm, MD, DDS, DVM or equivalent)
≥4
years of experience with 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
working within a global setting
Strong
understanding of external requirements related to regulatory documents
Experience
from the pharmaceutical /CRO industry
Relevant
experience with drug application processes to FDA and EMEA
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 +91 973 944 5518.
Deadline
20
November 2019
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