Manager, Clinical Data Scientist
IND - Chennai Office, India
INR 800K-1100K (estimate) Mid-level Full Time
Tasks
- Apply ALCOA principles
- Assure inspection readiness
- Coordinate CDIS deliverables for clinical trials
- Drive operational excellence with cross functional teams
- Ensure Trial Master File documents are filed contemporaneously
- Ensure adherence to data standards
- Ensure compliance with SOPs regulations and standards
- Ensure quality and timeliness of CDIS deliverables
- Establish study strategy timelines and resourcing
- Perform third party study data due diligence
- Provide leadership direction and oversight to data managers
- Provide oversight for data management plan
- Select and apply data acquisition standards
- Select quality risk indicators
- Serve as technical resource for collecting processing consuming reporting clinical trial data
Perks/Benefits
- N/A
Skills/Tech-stack
ALCOA | Clinical Trial Data | Clinical data | Clinical data management | Clinical trial | Data Acquisition Standards | Data Management | Data Management Plan | Data Standards | Data acquisition | Due Diligence | GCDMP | Inspection Readiness | Master File | Quality Risk Management | Risk Management | SOP compliance | Third Party | Third-party due diligence | Trial Master | Trial Master File | Trial data
Education
N/A
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