Senior CDC
at Icon plc
Ciudad de México, CDMX, Mexico -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 22 Sep, 2024 | Not Specified | 23 Jun, 2024 | N/A | Analytics,Data Validation,Clinical Data,Sme,Root,Functional Management,Management System | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
We have an incredible opportunity for a Senior Clinical Data Coordinator to join ICON’s Full Service Clinical Data Science team.
How To Apply:
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Responsibilities:
The Senior Clinical Data Coordinator supports and executes the data review activities, including data validation and analytics, that contribute to delivery of clinical data that meets agreed upon data integrity standards. They will act as the Data Review Team lead for one or more projects and act as Subject Matter Expert (SME) for various technologies or procedures within the scope of role.
- Support activities related to development of the Clinical Data Management System as needed
- Detect risks and signals in the data using quality indicators
- Accountable for the development of the CRF Completion Guidelines and supporting/reviewing other Clinical Data Science documents
- Perform root cause analysis of detected data issues
- Ensure study and task metrics are tracked and reported to Clinical Data Science Lead, project team, and functional management
- Manages third party data reconciliation process
- Collaborate with cross-functional and global groups
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Ciudad de México, CDMX, Mexico