The Senior Global Trial Associate contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs
Job Summary
The Senior Global Trial Associate contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.
Responsibilities involve a combination of execution and oversight to ensure deliverables and may include project management, study/project planning, conduct and management, and vendor/site payment processing.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.
Matching Summary
The Senior Global Trial Associate contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.
Salary
Base: zł223,020 - zł270,251; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Competitive benefits, services and programs
Skills & Requirements
Must-have
ICH/GCP compliance
clinical study execution
eTMF accuracy and completion
vendor management activities
study level documentation management
Nice-to-have
flexible to changing business demands
networking with key stakeholders
assessing situations and identifying paths
challenging the status quo
mentoring and coaching team members
Key Requirements
Minimum 2-4 years’ experience in Clinical Research
Experience in industry Clinical Trial Management Systems