The Sr CDM is part of the clinical study team, ensuring successful conduct and delivery of clinical studies to agreed timelines and budgets.
While data management activities are completely outsourced to vendors, the Sr CDM is instrumental in providing study-specific data management requirements during set-up, conduct and close out of clinical studies for different Health Relief and Health Wellness RB brands.
The Sr CDM is responsible for overseeing the vendor for all data management related activities.
The Sr CDM’s responsibility is to ensure data integrity throughout the study.
The Sr CDM ensures adherence to the RB data transparency policy and associated procedure.
Is this You?
You have a thorough understanding of the entire process of conducting a clinical study.
You are process-driven and able to influence without authority in a matrix organisation.
You are able to rationalize and manage different requirements related to the types of products being studies (IMP, medical devices, cosmetics & general products)
You can manage conflicting priorities with evolving and often challenging timelines.
You have a keen attention to detail and are service-oriented.
You have experience in managing communications with external vendors.
You have in depth and up to date knowledge of Good Clinical Practice and regulatory standards.
In Return RB offer very competitive salaries with excellent benefits and the chance to progress your career within a truly Global organisation.