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
Seniority
Mid Senior
Employment type
Contract
Work mode
On Site
Location
Woodcliff Lake, NJ, United States
Posted
10 years ago
GCPMedical CodingMedical TerminologyReconciliation
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.