Senior Clinical Data Manager

2 weeks ago

Nottingham, United Kingdom Worldwide Clinical Trials, LLC Full time

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality.Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
Why Worldwide
What Global Data Management does at Worldwide
Data Management is an ever growing and collaborative department. From start to finish, we are involved in clinical studies beginning with building the study database, to locking and delivering the final dataset for the project.Data Management reviews and ensures the clinical study data is of high quality for regulatory submissions.
The Data Management group is the perfect place to launch or further your career. Spanning various roles from data support staff, database and SAS programmers, coders and functional leads, there is place for you
To manage each of the data management projects to which assigned; provide leadership to the corresponding data management teams and to representWorldwide Clinical Trialsin all dealings with Sponsors with respect to the Data Management aspects of the projects to which assigned.
To write specifications for the set-up and modification of database and edit check specifications for assigned projects. Create and review project specific documentation for assigned trials, i.e. the Data Management Plan and the Data Management File and create and review CRF and eCRF completion guidelines, EDC system manuals and access instructions.
To produce information/reports directly from the clinical database or via the appropriate procedure to request a new report from the appropriate department or vendor.
To participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings. The job holder must be computer literate and numerate with a willingness to adapt to various computer systems.
It is essential that the job holder works with close attention to detail and is questioning about the validity of the data being entered and has an ability to phrase data queries in an understandable and impartial manner.
To have the ability to train new staff and to monitor their performance.
Proven project delivery skills.
Several years experience within Data Management or associated field.
For more information on Worldwide, visit or connect with us on LinkedIn .
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