Clinical Data Management Associate

#Hiring for Veeda Lifesciences

"Remote Opportunity"

Looking for "Clinical Data Management Associate"

Kindly drop your cv to - mahendra.t3705@veedalifesciences.com

Role & responsibilities

- Implements, monitors and supervises data management activities within assigned clinical trials, i.e., is responsible to design, create, validate, review, approve and maintain data management tool specifications, including but not limited to: Time & Events Schedules, eCRF Entry Guidelines, Edit Checks, Data Review Plans and Data Management Plans

Provides the study status updates with respect to data, using standard reports (CPT, data entry, queries, SDV, safety reconciliation etc.) and communicates efficiently the status to the team

Creates and executes data quality checks throughout the study conduct

Day to day responsibilities (under the guidance of senior personnel) may include but are not limited to:

• data review,
• open/close queries in the eCRF,
• medical coding,
• central lab data reconciliation,
• PK data reconciliation,
• ad-hoc data reports creation,
• User Acceptance Testing (UAT) of internal and external electronic Data Capture systems

Provides support to the resolution of issues and inputs ideas to help resolve issues and contribute to continuous improvement

Complies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection

Professional Experience Requirements

Required: 3 years' work experience as Clinical Data Manager in Phase I-III Studies

Desirable: Experience working with Medidata Rave