Why This Role Stands Out
This on-site Clinical Data Manager role offers a fantastic opportunity to deepen your expertise in data management across various study phases, contributing to impactful clinical trials within a reputable company. You'll thrive here if you possess strong project management skills, hands-on EDC experience, and a background in oncology data, making this an excellent next step in your career. Apply today to leverage your skills and advance your professional journey!
Quick Overview
Job Description
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.
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.
• 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.
This job is with one of my Financial Client.
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