Tasks:
- * Advise on clinical trial data collection, processing, consumption, and reporting
- * Collaborate with study teams, research units, and external data providers
- * Conduct third party study data due diligence
- * Coordinate clinical data science deliverables for clinical trials
- * Develop data management plans
- * Drive data quality and operational efficiency against study milestones
- * Ensure adherence to GCDMP and ALCOA principles
- * Ensure compliance with SOPs, regulations, and data standards
- * Ensure quality and timely delivery of clinical data management outputs
- * Establish study strategy, timelines, and resourcing with asset leads
- * Maintain high-quality, contemporaneous Trial Master File documentation
- * Oversee data managers supporting clinical trials
- * Represent Clinical Data Sciences on core study teams
- * Select and apply clinical data acquisition standards
- * Select quality risk indicators
Perks/Benefits:
Skills/Tech stack required:
[ALCOA principles] [Clinical data] [Clinical data collection] [Clinical data management] [Clinical data processing] [Clinical Data Quality] [Clinical data quality management] [Clinical data reporting] [Clinical data standards] [Clinical trial] [Clinical Trial Data] [Clinical trial data acquisition] [Clinical Trial Operations] [Data acquisition] [Data collection] [Data Due Diligence] [Data Management] [Data management plans] [Data Processing] [Data Quality Management] [Data reporting] [Data Standards] [Due Diligence] [GCDMP] [Master File] [Quality management] [Quality risk indicators] [Risk indicators] [SOP compliance] [Third Party] [Third-party data] [Third-party data due diligence] [Trial Master] [Trial Master File] [Trial operations]
Educational requirements:
N/A
Role(s):
[Clinical Data Manager] [Clinical Data Scientist] [Data Manager] [Data Scientist] [Manager] [Scientist]