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Job Specification Purpose - To action all tasks relating to Clinical Data Management from the start to the finish of a study. - To support Project Manager in studies across DM functions. Core Accountabilities: Activities required of a Clinical Data Coordinator I (however not restricted to) are as below - To assist in the testing of databases prior to activation. - To assist in the preparation of study specific documentation as appropriate. - To assist with the processing of clinical data for projects. - To critically review CRFs as specified in the Data Management Plan and to query any errors or omissions with either the study sponsor or the investigator as required. - To track and resolve Data Clarification Forms in the study specific Database. - To resolve Self-Evident Queries/Allowable Changes in the study specific Database. - To perform the Quality Control of Data Entry and CRF/database as appropriate. - To prepare any documentation for return to client/internal archiving at study

Job Specification Purpose - To action all tasks relating to Clinical Data Management from the start to the finish of a study. - To support Project Manager in studies across DM functions. Core Accountabilities: Activities required of a Clinical Data Coordinator I (however not restricted to) are as below - To assist in the testing of databases prior to activation. - To assist in the preparation of study specific documentation as appropriate. - To assist with the processing of clinical data for projects. - To critically review CRFs as specified in the Data Management Plan and to query any errors or omissions with either the study sponsor or the investigator as required. - To track and resolve Data Clarification Forms in the study specific Database. - To resolve Self-Evident Queries/Allowable Changes in the study specific Database. - To perform the Quality Control of Data Entry and CRF/database as appropriate. - To prepare any documentation for return to client/internal archiving at study

Purpose: - To action all tasks relating to Clinical Data Management from the start to the finish of a study. - To support Project Manager in studies across DM functions. Core Accountabilities: Activities required of a Clinical Data Coordinator II (however not restricted to) are as below: - To assist in the testing of databases prior to activation. - To assist in the preparation of study specific documentation as appropriate. - To assist with the processing of clinical data for projects. - To critically review CRFs as specified in the Data Management Plan and to query any errors or - omissions with either the study sponsor or the investigator as required. - To track and resolve Data Clarification Forms in the study specific Database. - To resolve Self-Evident Queries/Allowable Changes in the study specific Database. - To perform the Quality Control of Data Entry and CRF/database as appropriate. - To prepare any documentation for return to client/internal archiving at study completion

Job Specification Purpose - To action all tasks relating to Clinical Data Management from the start to the finish of a study. - To support Project Manager in studies across DM functions. Core Accountabilities: Activities required of a Clinical Data Coordinator I (however not restricted to) are as below - To assist in the testing of databases prior to activation. - To assist in the preparation of study specific documentation as appropriate. - To assist with the processing of clinical data for projects. - To critically review CRFs as specified in the Data Management Plan and to query any errors or omissions with either the study sponsor or the investigator as required. - To track and resolve Data Clarification Forms in the study specific Database. - To resolve Self-Evident Queries/Allowable Changes in the study specific Database. - To perform the Quality Control of Data Entry and CRF/database as appropriate. - To prepare any documentation for return to client/internal archiving at study

Roles and Responsibilities Core Accountabilities: Activities required of a Junior Data Process Associate (however not restricted to) are as below: To enter data from CRF’s into study database To follow applicable data entry guidelines. To scan CRF’s as requested To assist in the testing of databases prior to activation. To assist in the preparation of study specific documentation as appropriate. To assist with the processing of clinical data for projects. To perform the Quality Control of Data Entry and CRF/database as appropriate. To be aware of and to work to the standards appropriate to the study (CRO or customer). To advise on possible improvements to procedures and standards. To perform other reasonable tasks as requested by management. To perform other reasonable tasks as requested by management. Education Qualified to an appropriate standard, preferably to degree level in a life sciences subject. Desired Candidate Profile Fresher's(0-1 year experience) with knowledge in CDM PC s

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