Principal, Data Manager

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.

Job Description Summary

The Principal Data Manager ensures DM tasks for the assigned studies are performed on time and within budget, partners with Sponsors, clinical and statistics to develop the data collection specification from all data sources
The Senior Data Manager manages in-stream data flow activities and deliver a quality database in accordance with the project plan, leads and drive the DM team, and acts as the reference point for the Sponsor and the appointed person responsible for the project from the data management perspective.

Job Description

ROLE

The Principal Data Manager leads and drives the DM team, acting as mentor and coach and as the reference point for the Sponsor and the appointed person responsible for the project from the Data Management perspective, to develop the data collection specification from all data sources 

The Principal Data Manager manages in-stream data flow activities and deliver a quality database in accordance with the project plan, ensures DM tasks for the assigned studies are performed on time and within budget, makes recommendation for process improvement and/or new standards development. 

The Principal Data Manager is an effective input into strategic planning across the department and bridges scientific or medical knowledge to data management processes to ensure sound data collection tools, validations and integration to fit for purpose clinical datasets.

 

KEY RESPONSABILITIES

• Accountable for driving achievement of project milestones from study start up through to delivery of database

• Provide Data Management input into the protocol

• Design the Case Record Form and guide process for CRF approval

• Define and develop the Data Management Plan, Data Validation Plan and their annexes (e.g. Reconciliation Plan), with input from the study team

• Validation of the database and computerized checks, including SAS listings or SAS checks 

• For EDC studies, define the User Acceptance Test Plan (UAT) and execute the test activities in the test environment to ensure quality eCRF 

• For EDC studies, timely response to issues identified by the eCRF Helpdesk 

• Prepare CRF completion guidelines 

• Prepare study specific data-entry guidelines and train data-entry staff 

• Perform term coding for clinical studies, raise manual queries for uncoded terms as required 

• Query management: review discrepancies, review answered queries, resolve and close where appropriate, manage the data cleaning process including manual checks and Medical Review listings 

• Create and test import programs for electronic data received from external vendors 

• Perform timely data integration of CRF and non CRF data (data import from external sources) 

• Perform reconciliation of external data (e.g. SAE, Central Labs, ECGs etc) 

• Run and monitor study data progress reports including query management and take appropriate actions (e.g. escalation, re-training, etc), escalate any study issues within study team