The role provides essential global study management support to ensure timely, high-quality, and compliant study execution within the biotechnology industry
Job Summary
The role provides essential global study management support to ensure timely, high-quality, and compliant study execution within the biotechnology industry.
Candidates will partner with Study Managers to deliver start-up activities, manage risk monitoring, and escalate early warning signals with proposed solutions.
The position offers opportunities to specialize in processes supporting multiple study teams throughout their lifecycle while gaining varied experience in study management.
Matching Summary
The role provides essential global study management support to ensure timely, high-quality, and compliant study execution within the biotechnology industry.
Skills & Requirements
Must-have
Master's degree or equivalent clinical experience
Experience with global clinical trials
Proficiency in CTMS and eTMF systems
Vendor management and oversight skills
Risk-based site monitoring expertise
Nice-to-have
Strong collaborative communication skills
Proactive issue escalation and resolution
Process improvement and automation mindset
Cultural sensitivity for global teams
Curiosity and willingness to learn new tasks
Key Requirements
Master's degree OR Bachelor's + 2 years experience
1 year of biopharmaceutical clinical research experience
Experience working on global clinical trials
Knowledge of CTMS, eTMF, and EDC tools
Ability to maintain inspection-ready documentation