Clinical Database Analyst Job

Company Name:
Salary period: Annual
Additional classifications: Science
Senior Clinical Database Analyst needed for a contract opportunity with Yoh's client located in Woodcliff Lake, NJ.
Top Skills You Should Possess:
- Strong programming skills required with Oracle's EDC system
- Knowledge of programming in clinical trials area within pharmaceutical/biotechnology
What You'll Be Doing:
- Provide programming and technical support related to clinical trials, end users support, and troubleshooting using different modules of Oracle's EDC product, InForm for Data Management department.
- Design eCRF screens and develop programs for data validation checks.
- Perform formal QC process for all the design and development activities.
- Guide junior developers/designers for most efficient and feasible method in designing eCRFs and building edit checks.
- Develop standard and Ad-hoc reports and listings to support Clinical Data Management, Clinical Operations for data cleaning, data reviewing, and trial monitoring functions.
- Ensure all programming activities and processes performed are conducted according to the standard operating procedures, standards, and good programming practices.
What You Need to Bring to the Table:
- Strong programming skills required with Oracle's EDC system, InForm, Central Designer, COGNOS Reporting database, with proficiency in Central Designer tool, COGNOS, .NET technologies: ASP, ASP.NET, VB.NET; C#, XML, SQL, PL/SQL; Good knowledge of Oracle database structure
- Seven (7) years of experience in programming with at least three (3) years with systems and programming in clinical trials area within pharmaceutical/biotechnology companies in developing/managing clinical database design and related technical solution.
- Understanding of programming in clinical trials area within pharmaceutical/biotechnology area.
- Good knowledge of Coding process, central labs, local labs, CDISC, CDASH, SDTM, MedDRA, WHO Drug.
- Knowledge of IRT, Central Coding, IReview/JReview, Clintrial, SAS is a plus
- Knowledge of clinical data management process, randomization, clinical data entry, coding process, external vendor data processing,
- Knowledge of Regulatory Guidelines in terms computer system validation, 21 CFR part 11,GCP, computer system validation
Opportunity is Calling, Apply Now!
Recruiter: Chelsea Tevis
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Click here to contact us if you are an individual with a disability and require accommodation in the application process.

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