The Clinical Scientist supports medical monitoring and scientific tasks on projects, enabling the use of high-quality scientific data for timely decision-making during clinical study planning, execution, analysis, and reporting
Job Summary
The Clinical Scientist supports medical monitoring and scientific tasks on projects, enabling the use of high-quality scientific data for timely decision-making during clinical study planning, execution, analysis, and reporting.
Responsibilities include collaborating with medical and safety data review teams, responding to protocol questions, preparing medical monitoring plans, and participating in safety review meetings with sponsors.
The role involves conducting literature searches, contributing to protocol development and clinical study reports, and supporting quality assurance and eTMF maintenance.
Matching Summary
The Clinical Scientist supports medical monitoring and scientific tasks on projects, enabling the use of high-quality scientific data for timely decision-making during clinical study planning, execution, analysis, and reporting.
Skills & Requirements
Must-have
medical monitoring
scientific data analysis
Good Clinical Practice
ICH guidelines
clinical trial design
adverse event data review
Nice-to-have
proactive issue prediction
stakeholder influence
global team collaboration
advanced scientific degree
Key Requirements
Master’s degree in biomedical, life science or similar
3 years of clinical trial experience
2 years of directly relevant therapeutic area experience