Clinical Data Associate
Biostatistics and Data Management
Bangalore
The position
Perform data entry to the acceptable quality level. This should be carried out in accordance with the standard procedures and guidelines.
- Ensure efficient handling of CRFs as per NN SOPs and departmental requirements from receipt until archival.
- Ensuring the integrity of clinical trial databases
- Accountability and tracking of documents for each batch received and report any discrepacies to trail data manager.
- Data entry of clinical trial data into database with accuracy and speed.
- Scanning, and Cleaning of CRFs and other documents as per project requirements.
- Perform Hyperlinking and Bookmarking tasks of CRF’s/eCRF’s in order to make it ready for submission.
- Involve in archiving of Trial related documents to HQ or locally as per TMFArchive specification.
- Data Entry should be done with a DM perspective with reference to NN procedures and instructions and data entry guidelines in an acceptable standard.
- Depending on the trial characteristic and as per the trial requirements, the Clinical Data Associate should be able to handle Data entry requests for DM milestones like Safety Study Group meetings, Interim analysis etc
Perform data entry to the acceptable quality level. This should be carried out in accordance with the standard procedures and guidelines.
- Ensure efficient handling of CRFs as per NN SOPs and departmental requirements from receipt until archival.
- Ensuring the integrity of clinical trial databases
- Accountability and tracking of documents for each batch received and report any discrepacies to trail data manager.
- Data entry of clinical trial data into database with accuracy and speed.
- Scanning, and Cleaning of CRFs and other documents as per project requirements.
- Perform Hyperlinking and Bookmarking tasks of CRF’s/eCRF’s in order to make it ready for submission.
- Involve in archiving of Trial related documents to HQ or locally as per TMFArchive specification.
- Data Entry should be done with a DM perspective with reference to NN procedures and instructions and data entry guidelines in an acceptable standard.
- Depending on the trial characteristic and as per the trial requirements, the Clinical Data Associate should be able to handle Data entry requests for DM milestones like Safety Study Group meetings, Interim analysis etc
Qualifications
·
Bachelor’s degree preferably in Life
Science or comparable degree in computer science, Information Technology
clinical information management or equivalent qualification.
·
Min of 1 year Data entry experience;
preferably on clinical database systems.
·
Computer literacy and proficient in
Microsoft Office tools.
For more details follow link below
http://www.novonordisk.co.in/careers/careers-working-in-india/see-list-of-all-available-jobs.42006BR.External.html