Opening for freshers as Clinical Data Associate @ Manipal Acunova Ltd.
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.
Salary: Not Disclosed by Recruiter
Industry:Pharma / Biotech / Clinical Research
Functional Area:IT Software - Application Programming , Maintenance
Role Category:Other
Role:Fresher
Keyskills
Data Entry data processing data entry operator
Desired Candidate Profile
Education-
UG: Any Graduate - Any Specialization
PG:Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
- Open for CONTRACT TO HIRE position
- Any Graduate.
- Good typing skills with adequate speed and quality.
- Knowledge and understanding of ICH GCP.
- Knowledge and understanding of Standard Operating Procedures.
- Good technical knowledge of the CDM processes.
- Understanding of clinical data management applications.
- Understanding and implementation of project specific deliverables.
- Defect recognition sklls, inspection skills, attention to detail, visual inspection speed and accuracy.
- Good Excel, Word & computer skills.
- Quick understanding / good communication skills (Verbal/Written).
- Strong interpersonal skills within the team.
- Problem solving and analytical approach.
- Time management and proactive.
- Enthusiastic, motivated and innovative.
Click here to apply
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.
Salary: Not Disclosed by Recruiter
Industry:Pharma / Biotech / Clinical Research
Functional Area:IT Software - Application Programming , Maintenance
Role Category:Other
Role:Fresher
Keyskills
Data Entry data processing data entry operator
Desired Candidate Profile
Education-
UG: Any Graduate - Any Specialization
PG:Any Postgraduate - Any Specialization, Post Graduation Not Required
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
- Open for CONTRACT TO HIRE position
- Any Graduate.
- Good typing skills with adequate speed and quality.
- Knowledge and understanding of ICH GCP.
- Knowledge and understanding of Standard Operating Procedures.
- Good technical knowledge of the CDM processes.
- Understanding of clinical data management applications.
- Understanding and implementation of project specific deliverables.
- Defect recognition sklls, inspection skills, attention to detail, visual inspection speed and accuracy.
- Good Excel, Word & computer skills.
- Quick understanding / good communication skills (Verbal/Written).
- Strong interpersonal skills within the team.
- Problem solving and analytical approach.
- Time management and proactive.
- Enthusiastic, motivated and innovative.
Click here to apply
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