POSITION TITLE:
Clinical Data Managers (CDM)
Become a part of a growing CDM department with an extensive experience base. Working within a strong team environment, the CDM will have the opportunity to work on all aspects of a clinical trial. Utilize your skills and knowledge to create innovative solutions for trials in all phases and/or therapeutic areas. Work with diverse companies, personnel and technologies.
Tasks may include the following:
Design and/or review CRFs/eCRFs, write CRF Completion Guidelines, define and document Data Management Plan including the development of protocol-specific workflows; ensuring study processes are appropriate and consistent with SOPs.
Assist in the coordination of the build and testing of clinical databases including validation checks, validate clinical data, reconcile SAEs, and perform coding. Coordinate the study QC audit, and develop corrective action plan if necessary.
Develop and/or utilize reports to track study progress. Ensure timelines and quality expectations are met. Coordinate and manage multiple projects which may include ensuring quality and consistency in data validation and handling among projects in a drug or device development program.
How To Apply
To apply for a position, please send cover letter and resume to .