Job Description Create and maintain all clinical studies (approximately 100 studies) in CTMS on daily basis per data/reports received. All updates should be completed within 5 days of receipt of data/reports.
Provide necessary follow ups with the study team to ensure data completeness using the IMPACT reports and resolve any queries in a timely manner within 5 days.
Data to be created/maintained are:
Addresses, telephone, fax and e-mail contact information for investigators, IEC/IRBs, and other site personnel for each study
Company personnel for each study
Study level milestones, protocol design information, recruitment plan, etc.
Country level milestones, Regulatory Approval information, recruitment plan, etc.
Site level milestones, recruitment information, etc.
For studies where data loading is being handled, checks and follows with the study teams will be required if errors are found during the loading process. Resolution should be within 5 days.
Provide support to end-users directly or by channeling requests to CTMS colleagues as appropriate
Compliance check should be completed on monthly basis using the Quality Check reports and follow up with study teams for any missing and data quality issues.
Data cleaning, new data entry, or rectification needed in CTMS.
Desired Profile Qualifications :
Individuals Experience
Relevant experience in maintenance of computer-based records-
Previous experience in use of a clinical trial management system (CTMS) is preferable.
Individuals Specific skills
Computer literate, especially in use and management of databases and spreadsheets reports
Basic understanding of the use of electronic systems in regulated environments is preferable.
Basic understanding of clinical development processes is preferable.
Good organization skills.
Diligent and reliable
Reasonable competence in spoken and written English.
Individuals Problem solving
Able to recognise problems/potential problems and alert management and/or take action as appropriate.
Able to prioritize routine work
Education: Any Graduate
Experience 0 - 2 Years
Reference 5490465
Read More
Provide necessary follow ups with the study team to ensure data completeness using the IMPACT reports and resolve any queries in a timely manner within 5 days.
Data to be created/maintained are:
Addresses, telephone, fax and e-mail contact information for investigators, IEC/IRBs, and other site personnel for each study
Company personnel for each study
Study level milestones, protocol design information, recruitment plan, etc.
Country level milestones, Regulatory Approval information, recruitment plan, etc.
Site level milestones, recruitment information, etc.
For studies where data loading is being handled, checks and follows with the study teams will be required if errors are found during the loading process. Resolution should be within 5 days.
Provide support to end-users directly or by channeling requests to CTMS colleagues as appropriate
Compliance check should be completed on monthly basis using the Quality Check reports and follow up with study teams for any missing and data quality issues.
Data cleaning, new data entry, or rectification needed in CTMS.
Desired Profile Qualifications :
Individuals Experience
Relevant experience in maintenance of computer-based records-
Previous experience in use of a clinical trial management system (CTMS) is preferable.
Individuals Specific skills
Computer literate, especially in use and management of databases and spreadsheets reports
Basic understanding of the use of electronic systems in regulated environments is preferable.
Basic understanding of clinical development processes is preferable.
Good organization skills.
Diligent and reliable
Reasonable competence in spoken and written English.
Individuals Problem solving
Able to recognise problems/potential problems and alert management and/or take action as appropriate.
Able to prioritize routine work
Education: Any Graduate
Experience 0 - 2 Years
Reference 5490465
Read More
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