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For your reference, we have included the original job posting below.
Clinical Data Manager
Job Number:
43824006
Company Name:
Kforce
Job Location:
Boston, MA US
Job Category:
Management & Business
Clinical Data Manager
At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you. This allows you to stay just as dedicated and still strike a balance between work and home.
Currently, one of our top clients is in search of an exceptional Clinical Data Manager in Cambridge, MA. The Clinical Data Manager leads and manages project activities at study level at assigned client sites for Clinical Data Management and ensures efficient coordination among study teams and data management teams.
Specific Accountabilities: * Act as a single point of contact for all data management center deliverables during the Study Set-up, conduct and close-out phases * Create/Provide input to project Data Management Plan * Provide input/review the data management components in the protocol * Creation of the Case Report Form from global standards and creation of protocol specific case report form modules by coordinating with sponsor's protocol team and review of the same * Accountable for the creation/review/maintenance of the CRF completion guidelines, edit check specifications leveraging global standard validations * Accountable for database review, testing and UAT of edit checks for assigned studies * Accountable for monitoring study progress and timely locking and freezing of database. * Responsible for Project Management of the study and accountable for all study deliverables from end to end. * Ensure adherence to SOPs * Provide guidance and supervision to the study teams
