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Posted 3 months ago

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Clinical Data Manager

Woodcliff Lake, NJ, United StatesRemoteContract

AI Summary

Clinical Data Manager independently performs data management and database lock activities for clinical studies, oversees offshore CRO work, and manages global projects in a pharma/CRO environment.

About this role

Clinical Data Manager

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com.


Title: Clinical Data Manager
Location: Woodcliff Lake, NJ
Duration: 1 year (Extendable contract)


Responsibilities

• Independently performs all data management functions to ensure timely and quality database lock for studies Phase I-III.
• Perform data management activities for EDC studies conducted in-house as well as oversee activities of off-shore CRO handling outsourced projects (protocol review, CRF development, database set-up activities, data validation process; medical coding, SAE reconciliation, etc...)

Requirements:
• Minimum 3-5 years’ experience in Clinical Data Management within pharma or CRO environment.
• Bachelor degree or above in scientific or related field required. Commensurate experience in Data
• Management may be considered.
• Hands-on experience conducting all DM activities and possess strong project management and excellent interpersonal skills to independently manage a global project.
• Must have experience with EDC, Inform preferred but open to other EDC such as RAVE, etc. Experience in some Oncology preferred.
• Knowledge of I-Review/J-Review a plus.
• Significant hands on experience when performing DM tasks, particularly with regards to general data review, discrepancy management and external data reconciliation.
• Oncology experience is a must, especially when dealing with Tumor reconciliation (RECIST 1.1, IrRECIST mRECIST etc;)
• Proficiency on all related regulations, GCP, and Good Clinical DM Practice.
• Computer proficiency and knowledge of medical terminology.
• Strong oral and written communication skills.

Qualifications

• Minimum 3-5 years’ experience in Clinical Data Management within pharma or CRO environment.
• Bachelor degree or above in scientific or related field required. Commensurate experience in Data
• Management may be considered.
• Hands-on experience conducting all DM activities and possess strong project management and excellent interpersonal skills to independently manage a global project.
• Must have experience with EDC, Inform preferred but open to other EDC such as RAVE, etc. Experience in some Oncology preferred.
• Knowledge of I-Review/J-Review a plus.
• Significant hands on experience when performing DM tasks, particularly with regards to general data review, discrepancy management and external data reconciliation.
• Oncology experience is a must, especially when dealing with Tumor reconciliation (RECIST 1.1, IrRECIST mRECIST etc;)
• Proficiency on all related regulations, GCP, and Good Clinical DM Practice.
• Computer proficiency and knowledge of medical terminology.
• Strong oral and written communication skills.


Additional Information

This job is with one of my Financial Client.

Skills

Clinical Data ManagementData ValidationDiscrepancy ManagementEDCGCPInformI-ReviewJ-ReviewOncologyRAVE

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