Job Description
1.To design, test, and maintaining of the project database, and the definition of data entry conventions.
2.To develop and validate the programs for comparing double data entry, listing individual data and applying edit checks.
3.To set-up external data import and validation as per agreed specifications.
4.To set-up clinical data coding programs / screens as per DM plan.
5.Provide technical expertise to the CDM team.
6.To file study documentation.
7.To perform other duties assigned by management.
8.To identify, communicate and resolve data issues on a timely manner.
9.To implement defined quality control procedures as per DM Plan.
10.To implement or adhere to SOP / regulatory requirements.
11.To liase with other project team members.
12.To record all activities accurately on the company standard timesheet.
13.To provide training to new team members.
Desired Candidate Profile
Should be Fluent in English, both written and verbal
Should have working experience in CDM systems such as Clintrial/Oracle Clinical/Inform etc
Should processes excellent programming skills in Oracle tools such as SQL, PL/SQL or SQL*PLUS and SAS
Should have good knowledge of web technologies such as JAVA, HTML, ASP etc
Should have good knowledge of drug development processes, ICH guidelines, CDM processes etc
Experience:1 - 2 Years Location:MumbaiEducation:UG - B.Pharma - Pharmacy;B.Sc - Any Specialization;BCA - Computers PG - Any PG Course - Any SpecializationContact:
Job Location :-Mumbai
Email: jalpa.pandya@mafoi.com
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