Thursday 1 March 2012

[Outsource:60169] Req: 5227 - Clinical Database Analyst **Baltimore MD**

Hi Associates,

Please check the below requirement and let me know if you have any consultants available. Please send me the updated profile to  vikas@bitsft.com

 

Clinical Database Analyst

 

Baltimore MD

9+ Months

 

Job Description:

Primary responsibilities include database design, development, implementation and maintenance for clinical trials. The Clinical Database Analyst will be the primary architect of the database(s) for the projects for which they are assigned, working closely with the Clinical Research Associate (CRA) for the project. In addition to database design and development, the Clinical Database Analyst is responsible for assuring the integrity and accuracy of data collected in the database. This includes developing and maintaining forms for electronic data entry.

Primary Responsibilities: DUTIES AND RESPONSIBILITIES:

• Plans, coordinates and performs database design, development and implementation for assigned clinical trials projects. Ensures that data security and integrity is maintained.

• Develops electronic data entry forms and/or data entry screens for the database. Programs case report forms (CRFs) for validation of the data prior to its entering the database.

• Provides tools for data conversion of existing data into new database management systems, as required.

• Develops edit checks and/or queries to validate (''clean up'') data that has been entered into the database.

• Develops, documents and implements validation test plans for various database components, including the electronic case report forms, and any queries or stored procedures written for the database.

• Defines and implements standard summary reports in graphical and/or tabular format. Assists and educates users in running and interpreting results from these reports.

• Assists statisticians and other programmers in understanding the database when they are generating specialized reports from the database. Assist in testing the validity of the data on the specialized reports.

• Maintains data management plan documentation of each database including, but not limited to, Database Diagram, Data Dictionary, Data Entry, Post-Data Entry, and CRF specifications.

 

Skills/Education Required:

• Strong knowledge of SQL (Structured Query Language) or other data retrieval languages is required.

• Strong knowledge of clinical trial/data management systems (e.g. Clindex, Clintrial, Phase Forward, Oracle Clinical) is required.

• Strong knowledge of relational database management systems (e.g. Oracle, SQL Server) is a plus.

• Working knowledge of electronic data capture (EDC) is a plus.

• Working knowledge of electronic data entry systems, specifically Teleform software, is a plus.

• Familiarity or knowledge of Visual Basic or PowerBuilder is a plus.

• Working knowledge in database design and database design software. Familiarity with a database design software such as ERWin, PowerDesigner, Visio, or System Architect is a plus.

• Working knowledge of Windows operating systems.

• Strong interpersonal skills, demonstrated capability of working on multiple projects at one time.

• Strong oral and written communication skills.

• Strong problem solving skills.

• Demonstrated project management skills.

 

Work Experience:

• B.S., M.S. in Computer Science, Software Engineering, Information Technology, Statistics, Life Sciences or related field and minimum of 3 years of relevant experience supporting clinical trials. Equivalent education or experience will be considered.

• Scientific background is preferred.

 

 

 

 

Thank You!

 

Vikas Jain

Bitsoft International Inc.
phone: 630.206.4036 | fax: 630.596.9069

2272 W. 95th St., Suite 220 | Naperville | Illinois, 60564 USA | bitsft.com

 

 Connect with me

View and apply to our open jobs at http://www.SkillGalaxy.com

 

We are "Certified Minority Owned Business Enterprise"

 

P Save trees, Print Only When Necessary

We respect your online privacy. This is not an unsolicited mail. Under Bills.1618 Title III passed by the 105th US Congress this mail cannot be considered Spam as long as we include contact information and a method to be removed from our mailing list. If you are not interested in receiving our e-mails then please reply with: REMOVE" in the subject line and your ID will be removed from our mailing list. We are sorry for the inconvenience caused to you.

 

No comments:

Post a Comment