Clinical Data Coordinator CoreLab Partners
THIS JOB HAS EXPIRED
Overview: Coordinates the development and implementation of clinical data management project deliverables according to RadPharms Standard Operating Procedures (SOPs).
Responsibilities:
Review and reconcile data discrepancies within clinical databases
Generate and manage data clarification forms for query resolution
Expertise with protocol, charter language and transfer plan creation and review
Serve as data management representative for a set of assigned studies; liaise with CDM customers representatives; attend internal and external sponsor meetings
Participate in efficiency and quality improvement initiatives
Create and update data management documentation as appropriate
Manage the data collection, review, and cleaning process for assigned studies
Create and review Data Entry Instructions and Data Review Guidelines under minimal supervision of senior staff
Coordinate the creation and revision of forms and source documents under minimal supervision of senior staff
In conjunction with the Oracle Clinical team, participate in the creation, design and validation of clinical databases, including but not limited to the testing of the data entry application,
creation and testing of standard and study specific validation procedures under minimal supervision of senior staff
Perform data entry as needed
Perform quality control review of data
Review clinical data pre and post-extraction for accuracy and completeness prior to transfer with minimal supervision of senior staff
Coordinate multiple studies simultaneously with minimal supervision of senior staff
Provide training to new employees under supervision of senior staff
Perform data transfers for all applicable modes of transfer with minimal supervision of senior staff
Actively participate in cross-functional Study Teams
Represent the department and company professionally outwards
Qualifications:
Undergraduate degree in life science, allied health, or related field preferred and/or minimum 2 years relevant Clinical Data Management industry experience required
Proficient with Microsoft Office (Word, Excel, PowerPoint), Adobe Acrobat Professional
Prior CDC/CDM experience with industry standard clinical data management systems (Oracle Clinical, Clintrial, EDC/RDC) preferred
Experience with Diagnostic Imaging and Oncology Trials a plus.
Working knowledge of GCPs
Excellent written and oral communication skills
Must be able to prioritize independently depending on project timelines and urgency
Initiative for improvements is expected
Responsible and detail oriented with a co-operative and flexible attitude
| Location: |
100 Overlook Center
Princeton, NJ 08540
United States
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THIS JOB HAS EXPIRED