Principal II, Business/Medical Intelligence & Analytics
Principal II, Business/Medical Intelligence & Analytics
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
1. Simultaneously leads trials as a Trial Data Manager for 4 trials in parallel with minimal to no support.
2. Demonstrates a business understanding of the portfolio products and indication to identify and assist in successful application of data management processes
3. Provides feedback to assure well-written protocols. Recognize and resolve protocol issues that may impact database design data validation data integrity and/or analysis/reporting while making the best use of standards and best practices
4. Leads the team through database build requirements timelines and complete startup activities for study including: building the eCRF completion guidelines standard and simple rules data validation plan and user acceptance testing (UAT). Overseas and ensures quality where support services are provided.
5. Set up and Manage external data in accordance with protocol requirements process and validation requirements
6. Performs DM maintenance and validation activities during the course of the study timely and with quality and overseas and ensures quality where support services are provided.
7. Ensures that Clinical Coding is performed at a consistently high standard in the Therapeutic Area/Franchisee. Ensures that the Coding related sections of the Data Management Documents are updated and Coding is complete and reviewed in support of all timelines/deliverables
8. Tracks and reports status and progress for assigned trials and projects. Is proactive to ensure milestones are met with quality (incl. Snapshots and interim/final locks).
9. Effectively communicates status updates and study level information to the Clinical Trial Team (CTT) and Program Clinical Data Manager (PCDM). Represents Data Management at cross functional forums meetings and provides timely feedback to partners
10. Responsible and accountable to ensure consistency of assigned trials with program level standards through technical implementation of Industry (CDISC and regulatory) Data Standards while acting as a technical consultant providing standards input to all relevant area data management and reporting areas.
11. Coaches and mentors associates as required ensures that DM associates on the program are aware of the risks priorities goals and impact of the work contribution.
12. Provides effective input into DM initiatives and innovations for quality efficiency and continuous improvement in scientific and operational excellence
13. Understands Health Authority requirements and ensures adherence to GCP standards SOPs/procedures job aids and guidelines and is able to prepare for and participate in Health Authority inspections and audits as required
14. Maintain up-to-date knowledge of relevant technologies (EDC software languages applications etc.) Industry Standards (e.g. CDISC eCTD etc.) and regulatory guidelines.
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon please click the appropriate link below to apply on the Internal Career site.
Find Jobs for Contingent Worker
Alcon is an Equal Opportunity Employer and takes pride in maintaining a diverse environment. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of race color religion gender national origin age sexual orientation gender identity marital status disability or any other reason.
Required Experience:
Staff IC
Employment Type
Full-Time
