Novo Nordisk Associate
Manager for Medical Writer in Global Development Master’s / Phd in Life
Science, Medicine, Veterinary science etc
About the
department
Clinical
Reporting is the medical writing function at Novo Nordisk and is a part of
Global Development. Global Development is responsible for managing clinical
drug development worldwide, from early development phases to market
authorisation as well as life cycle management of our approved products.
Clinical
Reporting consists of 6 departments in Soeborg, Denmark, with around 90
colleagues and 4 departments in Bangalore, India, comprising around 40
colleagues. We cover medical writers, disclosure professionals and clinical
publishers, and pride ourselves on a diverse cultural and professional
background.
The Medical
Writing unit in India has seen a tremendous growth curve and has become an
integral part of the Global Clinical Reporting community in a short span of 9
years, since its inception in 2011. It is a dynamic mix of young, enthusiastic,
qualified and skilled Medical Writers, Disclosure Professionals 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
As an
Associate Manager, you will be responsible to lead, and drive deliverables
related to Insulin and obesity project area of Medical Writing in Novo Nordisk,
and to set directions and manage the teams to meet the department and
organisation's business goals according to Novo Nordisk Way. You should ensure
effective coaching and mentoring of team members to enhance performance and
support individual development. You will plan resources for all deliverables
from the teams and support department head in ensuring optimal and flexible use
of resources. Furthermore, you will drive continuous improvement and quality
mind-set with compliance to Novo Nordisk Quality Management System.
An important
aspect of the role is to take part in the development of the Global Medical
Writing environment with respect to competencies, systems, procedures and
global collaboration. Global knowledge-sharing and harmonisation of medical
writing processes are key elements for improved efficiency and continued
success. Overall, the job requires an independent, committed and
result-oriented person. Novel approaches to resolve resource, competency,
technical and organisational issues and constraints are required. Frequent
travelling to attend meetings with stakeholders in Denmark is part of the job.
The ability to work in a global context is important, as well as cultural
awareness and inclusive approach.
Qualifications
We are
expecting you to hold the below skills and knowledge:
Master’s /
Phd in Life Science, Medicine, Veterinary science etc. or equivalent
professional experience
Minimum 5
years of experience in scientific and medical publications, regulatory
documents etc.
2-3 years’
experience in people management either from project or line management is
preferred.
Thorough
understanding of drug development, ICH GCP, ICH E3 and other regulatory
requirements.
Experience in
Life Cycle Management of established products is preferred.
Clear
communicator with great stakeholder management skllls
Set
direction, lead and motivate your team to deliver its best and have a desire to
influence and impact others beyond your own area.
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