Senior Clinical Data Analyst (Medical Device)

On-site

Responsibilities

Perform all data management tasks as appropriate to include, but not to be limited to data review and query management to ensure that quality standards (both internal and client) are achieved within stipulated timelines.
Generate, resolve and track queries to address problematic data identified during aggregate data review activities.
Run and execute additional programs, special listings, reconciliation discrepancy listings etc.) used to support the review of clinical trial data.
Modify standard templates to create study specific Data Management Plans, or eCRF completion guidelines.
Support team members by creating forms/memos as required.
Generate study status reports.
Perform database extracts.
Support the training of new staff on project specific Data Management processes.

Responsibilities: Ensure that all allocated projects are carried out in strict accordance with the relevant protocols, global harmonized SOPs, and the specified standards of GCPs.
Qualifications (Minimum Required): University / college degree (life sciences, health sciences, information technology or related subjects) or a certification in allied health professions from an appropriate accredited institution.
experience in clinical research (Data management preferred). Additional
Experience with clinical EDC.
Knowledge of medical terminology.
Knowledge of effective clinical data management practices. *Please submit your English CV Learn more about our EEO & Accommodations request here .

Join Fortrea's Medical Device and Diagnostics team and make a difference as Clinical Data Analyst! Job Overview: Serve as a member of the project team with primary responsibility for coordinating the clinical data review, query generation / resolution and reconciliation activities to support the Data Management lead with the delivery of clinical data according to client quality and integrity specifications, project timelines and productivity targets.