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The Client Neuroscience Group Business is looking to fill a Senior Manager, Data Operations opening at its North American Headquarters in Woodcliff Lake, NJ.

Direct Hire - Senior Manager, Data Operations in Woodcliff Lake, NJ at Integrated Resources, Inc

Date Posted: 5/8/2019
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Job Snapshot

* Employee Type:
Full-Time
* Location:
Woodcliff Lake, NJ
* Job Type:
Management
* Experience:
Not Specified
* Date Posted:
5/8/2019

Job Description

NEUROLOGY
Senior Manager, Data Operations - Neurology Business Unit

Job Description

The Client Neuroscience Group Business is looking to fill a Senior Manager, Data Operations opening at its North American Headquarters in Woodcliff Lake, NJ.

Responsibilities include but are not limited to:

- The individual should have expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML.
- Excellent technical skills in EDC and SAS systems and application development.
- Experience in consulting on projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle at global level for both CRF standards and SDTM standards.
- Experience in Review and Quality assurance of datasets and programming specifications produced by other programmers.
- Experience in accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analyses and submissions.
- Responsible for implementing new technologies for end users and streamlining the process from data collection to submission.

Job Requirements:

- Bachelor's degree in life sciences or technology field required.
- Must possess 7 or more years of relevant programming and application development experience in CRO, pharmaceutical or biotech organizations.
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The individual should have expertise in addressing technical challenges that connect EDC, SAS, CDISC and XML. - Excellent technical skills in EDC and SAS systems and application development. - Experience in consulting on projects dealing with the assessment, design and/or implementation of CDISC data standards in the clinical data life cycle at global level for both CRF standards and SDTM standards. - Experience in Review and Quality assurance of datasets and programming specifications produced by other programmers. - Experience in accountability for development and maintenance of cross-functional / cross-department process related to clinical trials SDTM data production, including specification, programming, QC, and deliverables of SDTM data for analyses and submissions. - Responsible for implementing new technologies for end users and streamlining the process from data collection to submission., Bachelor's degree in life sciences or technology field required. - Must possess 7 or more years of relevant programming and application development experience in CRO, pharmaceutical or biotech organizations.



* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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