Clinical Data Manager Jobs
Plainfield, NJ
| As part of a clinical working group, the Sr. Clinical Data Manager (CDM) is responsible for the accuracy and completeness of the clinical data collected during a clinical trial. With the appropriate level of experience, the Sr. CDM will manage one or more trials of moderate to high complexity or scope and will coach/mentor junior CDMs on the project. At the trial level and across trials, the Sr. CDM will perform and often coordinate the following activities:
development of data specifications for the eCRF (including leading the review meeting), coordination of the UAT of eCRF and other tools, development of the Data Management Plan, (including leading the review meeting), data review, query generation, data coding, electronic data reconciliation, identification of protocol deviations and oversight of activities performed by a CRO or vendor. Requirements A minimum of Bachelors Degree or equivalent industry (Pharmaceutical, Biotech and/or CRO) experience required; life sciences background preferred. A minimum of 5 years of pharmaceutical or health care experience required. Clinical Data Management experience from within the industry is required. Experience with eDC (electronic data capture) is preferred |
