Person2Person, LLC
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| Clinical Database Analyst Based in Northern, NJ |
| Outstanding Contract opportunity with a global pharmaceutical Company focused on multiple therapeutic areas including Neurology, Oncology and Critical Care. They continue to move forward with an entry into biologics with the development of therapeutic antibodies and other such agents, which contributes to their innovate drug discovery process. Be a part of this global market leader! |
| SCOPE & DUTIES |
* Design, build, test, deploy, and manage assigned Oncology EDC trials using Oracle’s EDC product,
InForm.
* Design eCRF screens and build rules for data validation checks using Central Designer in InForm.
* Provide advanced level programming and technical support, end users support and trouble shooting
for Data Management department within Oncology Product Creation Unit with quality and efficiency.
* Guide junior developers/designers for most efficient and feasible method in designing eCRF's and edit
checks.
* Develop standard, Ad-hoc reports, and listings within InForm to support Clinical Data Management,
Clinical Operations for data cleaning, data reviewing and trial monitoring functions.
* Collaborate with external vendors/PDMs to develop and maintain external data transfer specification,
data transmission, testing, and data loading.
* Ensure all programming activities are performed following the departmental standards and guidelines.
* Perform user management, coordinate User Acceptance Testing, and production roll out activities for
individual trials.
* Perform post production changes.
* Liaise with vendors to resolve and follow-up outstanding / escalated technical issues.
* Manage the assigned projects independently within established timelines.
| REQUIREMENTS |
* Strong programming skills required with Oracle’s EDC system, InForm, Central Designer, COGNOS,
with proficiency in Central Designer
tool, COGNOS, C#, XML, SQL, PL/SQL; Good knowledge of ORACLE database structure
* At least 7 years of experience in programming with at least 5 years with systems and programming in
clinical trial area in
developing/managing clinical database design and related technical solution.
* Understanding of standards specific to clinical trials in the Oncology area, Good knowledge of Coding
process, central labs, local
labs, CDISC, CDASH, SDTM, MedDRA, and WHODRUG.
* Knowledge of IRT system, ClinTrial, and SAS is a plus.
* Knowledge of clinical data management process, randomization, clinical data entry, coding process,
external vendor data processing is required.
* Good understanding of clinical data handling process in Oncology area is needed.
| Executive Recruiting Specialists in the NY/NJ/CT Region |
Apply today! For immediate consideration, please email resume to: lsydor@person2personllc.com |