Novo
Nordisk Project Manager for Clinical Development Centre degree within life
science or healthcare
About the department
Clinical Development
Centre Denmark (CDC India) is a new organisation in the Clinical Research
Department is connected to the India affiliate. The CDC India is responsible
for planning, execution and finalisation of clinical trial activities e.g.
project management and administrative tasks related to conduct of the clinical
trials in close collaboration with the adjacent affiliates across India,
Malaysia and Thailand. In Clinical Development Centre (CDC) India we
are approximately 10-15 highly skilled and ambitious employees, Trial Managers
and Clinical Trial Administrators. We value an open, trust-based and creative
working environment as well as a great team spirit. Our working environment is
characterised by interesting and demanding assignments and continuous
professional development opportunities.
The position
As Project Manager you
will be an essential member of the CDC India team supporting entire clinical
trial Project Management tasks for assigned CDC Trials. You will be expected to
drive a broad range of tasks that ensure successful and on time trial progress.
You will collaborate with
many internal partners such as adjacent affiliates, Clinical Research
Associates, Clinical Trial Administrators, Headquarter International Trial
Managers and other Novo Nordisk colleagues.
You will be leading the
international team of Clinical Research Associates within your assigned trials,
focusing on stakeholder engagement, knowledge sharing, monitoring of trial
progress and decision making within trial execution.
You will be part of the
CDC Project Managers team, which is managed out of India. A very important part
of the Project Manager role is that you enjoy and are able to travel both
domestic and International around 4-5 days in a month average and as when
required.
The job also requires
that you apply a structured and analytical approach to processes and trial
documents, such as recruitment strategies and follow-up, risk analysis and
risk-based monitoring plans, patient retention plans, monitoring visit reports,
communication plans, quality oversight in trial execution and trial budgets.
Qualifications
Below are the required
skills.
- You hold an academic degree within
life science or healthcare
- You have solid knowledge and
at-least 5 years’ experience in clinical trial Management including
Clinical Trial Monitoring, Local trial Management and well versed with
CTMS tools IMPACT, RBM (Qlik Sense), eDC (inform), novoGlow, IWRS,
Clincost etc
- Further, you have experience in
working with many stakeholders across nationalities and cultures. The job
requires high proficiency in English
FOR MORE JOB UPDATES
No comments:
Post a Comment