Opening for the post of Clinical Data Associate post @ Manipal Acunova Ltd
Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries.
Job Title : Clinical Data Associate
Eligiblity : B.sc/M.sc Life science / Clinical Research
Experience : 0-2 years
Job Description :
Receive/track and Enter the CRF data.in compliant with SOW/sponsors specifications/process and SOPs and adhere to the timelines and project specific instructions set by PDM.
Report and collect all the missing data in time in co-ordination with PDM to fecilate speedy completion data entry.
To participate and give input for process optimization in alignment with the SOW and sponsors requirement.
Periodic assessment of goals and objectives set for the role.
Understanding the scope of work and provide input for all the study set up activities.
Validation of data entry screens using the full dummy data and documentation.
Ensures all CRFs sent from the Clinical Trial site is received & tracked .
Generation of tracking DCFs for the discrepancies identified in the CRF tracking process.
Ensures data entry in the clinical database as per sponsors specifications/process/ DE guidelines and SOPs.
Ensures and uses various data entry method to encode data from the CRFs into CDMS.
Ensures to securely storage/filing of all SDDC.
Quality control plans.
Generation of status report periodically (for internal requirement/for sponsor requirement) as requested by PDM.
Participating and attending in various inter-departmental workshops as a means of process improvement and knowledge share.
Timely updation of Work Plan to have update on CTQs and goal & objectives
Click here to apply
Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries.
Job Title : Clinical Data Associate
Eligiblity : B.sc/M.sc Life science / Clinical Research
Experience : 0-2 years
Job Description :
Receive/track and Enter the CRF data.in compliant with SOW/sponsors specifications/process and SOPs and adhere to the timelines and project specific instructions set by PDM.
Report and collect all the missing data in time in co-ordination with PDM to fecilate speedy completion data entry.
To participate and give input for process optimization in alignment with the SOW and sponsors requirement.
Periodic assessment of goals and objectives set for the role.
Understanding the scope of work and provide input for all the study set up activities.
Validation of data entry screens using the full dummy data and documentation.
Ensures all CRFs sent from the Clinical Trial site is received & tracked .
Generation of tracking DCFs for the discrepancies identified in the CRF tracking process.
Ensures data entry in the clinical database as per sponsors specifications/process/ DE guidelines and SOPs.
Ensures and uses various data entry method to encode data from the CRFs into CDMS.
Ensures to securely storage/filing of all SDDC.
Quality control plans.
Generation of status report periodically (for internal requirement/for sponsor requirement) as requested by PDM.
Participating and attending in various inter-departmental workshops as a means of process improvement and knowledge share.
Timely updation of Work Plan to have update on CTQs and goal & objectives
Click here to apply
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