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Experience:3+ years
Location:NJ - Northern

Our Direct Client in NJ is looking for a long term Contract CDM.
Please email me for further details: phillips44@aol.com.
Thank you,
Ted Phillips


• Candidate will provide comprehensive data management expertise to Data Management to provide efficient, quality data management products that meet customer needs
• Serve as the Lead Data Manager on in-house studies
• Customer negotiation on timeline, budgetary and other data issues
• Develop presentations and present at investigator meetings
• With minimal guidance, manage delivery of projects through full data management process life-cycle
• With minimal guidance, manage project timelines and quality issues, and identify and justify out-of-scope
• Provide input for negotiations with vendors
• Manage outside vendors
• Complete external data reconciliation (i.e., ECG data)
• Complete ongoing laboratory reconciliation
• Provide comprehensive data management expertise (including all operations tasks and DMP generation
oversight and approval)
• Oversee the development of CRFs
• Perform comprehensive quality control procedures
• Communicate ideas for process improvement
• Provide input in developing and implementing new technology
• Understand and comply with core operating procedures and working instructions
• Meet objectives as assigned
• Some knowledge of CDISC standards
• Develop and maintain good communications and working relationships with Project Team
• Interact with Project Team members to negotiate timelines and responsibilities as well as track overall timelines

• Bachelor’s degree in clinical, biological, or mathematical sciences with a minimum of 5-7 years of experience in a clinical data management role
• Thorough knowledge of the data management process
• Hands on experience in running in-house studies
• External Data Capture (EDC) experience
• Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology
• Previous experience and proven competence in managing delivery of project through full data management study life-cycle (phase I and Phase II or Phase III).
• Comprehensive understanding of clinical drug development process
• Excellent organizational, communication, and data management skills (detail oriented)
• Ability to establish and maintain effective working relationships with
coworkers, managers, and clients

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