Clinical Data Manager
Mindlance
Apply to this job Woodcliff Lake, NJ, us on site Until 8/21/2026 First posted February 23, 2026 Last posted February 23, 2026
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.
About this role
Summary
Manage clinical data for oncology studies, oversee data review, validation, and reconciliation processes.
Job title
Clinical Data Manager
Experience level
3-5 years
Industry
pharmaceuticals
Location requirements
Woodcliff Lake, NJ; on-site role, no remote work
Salary
Not specified
Management role
No
Skills & keywords
Required skills
clinical data managementEDCGCPmedical terminologyoncology
Preferred skills
RAVEI-ReviewJ-ReviewRECIST 1.1IrRECIST
Specializations
oncologyEDCdata reviewreconciliationtumor
Locations
Structured locations inferred from the posting.
Woodcliff Lake, NJ, USA
On-site City