This is a unique opportunity to work directly with a leading global pharmaceutical company. Utilising your Data Management knowledge and skills to lead teams and clinical studies to success.
Working directly within the sponsor teams you’ll serve as an extended team member of the evidence team and will be responsible for oversight of all data management (DM) related communications, specifications, and documentation that includes but not limited to the Data Management Plan (DMP).
The GDML is responsible for the overall quality and integrity of the database, and they work
collaboratively to ensure that all Clinical Data is collected, managed, and reported clearly, accurately,
and securely based on the study’s protocol and to the highest scientific industry standards.
You’ll be responsible for several studies depending on a given therapeutic area, size,
complexity and working model.
Key Responsibilities include :
Essentially the team is looking for driven, data management professional with good leadership qualities. Someone with a good understanding of clinical EDC systems and GCP knowledge.
The role will require you to be a strong communicator and be able to work within a team environment as well and being independent.
If you fit these skills and requirements and want to push your career forward within one of the world’s leading pharmaceutical companies, we welcome your application.