About the Company
The company have more than 1400 people and work across the country with many functions and this position directly reports to manager. The company is a Danish MNC with offices in more than 8 countries production facilities. The firm have offices in more than 5 countries. The firm have Tresiba, Insulated type of products. The firm have more than 100 years of experience in Insulin production. The company have many sophisticated technologies like gene editing, stem cells technology and proteins peptide sequencing. The company have products in all the stages of pipeline that is in 4 phases.
About the Job
Experience: 12+ years experience with a minimum of 5 years of experience in clinical trial conduct and need to have bachelor degree in pharmacy, natural science and computer science
Requirement:
As a Ranking director, the ideal competitor will be important for the Preliminary Information The board Discs GBS supervisory group. This will include collaborating and expecting new difficulties and requirements for the division, and fostering the cycles in the association as needs be, as well as guaranteeing ceaseless improvement. The ideal competitor will be liable for the presentation of their groups and nature of their work while in consistence with ISO, SOPs and administrative rules which straightforwardly affects the crucial opportunity to advertise for new medications .
The up-and-comer will be liable for all worldwide information the board exercises (incl. data set-up exercises, information dealing with and oversight) across the stage 2-4 Other Serious Persistent Sicknesses (OSCD) and Results preliminaries in Novo Nordisk. Extra obligations include:
Add to the worldwide asset designation, guaranteeing that preliminaries are provided with Clinical Preliminary Information Chiefs sooner rather than later.
Guarantee a ceaseless improvement outlook by partaking in quality exercises, criticism meetings and examples learned.
Plan and lead division gatherings, raise significant issues and illuminate important gatherings, and add to the overall data stream nearby.
Deal with the division as per the Novo Nordisk way including fostering the workers and the group to meet Novo Nordisk business needs.
Speaking with different partners and capacity to work in a worldwide climate.
Staying aware of industry patterns to drive development and change inside the division.
Contribution to protocols
Obligation regarding information assortment instruments, for example eCRF, patient journals, wearables and others
Dealing with and cleaning of information through the lifecycle of a preliminary
Arrangement of informational collections for outer information checking boards and entries
Support in administrative reviews
Overseeing dangers and issues and actually imparting applicable situations with partners