Manager / Associate Manager for Medical Writer in Global Development
We are looking for a Manager 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
Your key responsibilities will be to lead and drive deliverables related to Novo Nordisk compliance with disclosure requirements, also 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.
The role involves prioritising and managing diverse tasks and stakeholders, often only with general guidelines available for the tasks to be performed. Consequently, a great deal of self-initiative is demanded as well as flexibility and resilience. 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 Headquarter is part of the job. 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.
- Master’s / Phd in Life Science, Medicine, Veterinary science etc. or equivalent professional experience
- Minimum 1-3 years of experience in reporting and distribution of results from clinical trials, scientific and medical publications, regulatory documents etc. Preferred
- 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 registration and disclosure of studies in public registries is preferred
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 Hemanth / Ganesh Shetty at hmku@novonordisk.com / gsy@novonordisk.com
Deadline
30 August 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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