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Tier-1 pharma employer, metro location, and a generalist clinical delivery role increase competition.
Requires clinical trial and regulatory experience in biotech/CRO, so skills are not easily transferable.
Explicit years thresholds plus mandatory clinical trial, CTMS, and regulatory experience make shortlisting strict.
Provide global study management support to clinical study teams ensuring timely, high-quality, compliant execution.
Own specific study tasks including start-up activities, risk monitoring, issue management, and vendor coordination.
Maintain and monitor clinical trial systems and documentation to ensure accuracy and inspection readiness, supporting data flow and recruitment strategies.
Master’s degree OR Bachelor’s degree with 2+ years clinical execution experience OR Associate’s degree with 6+ years clinical execution experience OR High school diploma with 8+ years clinical execution experience.
At least 1 year of biopharmaceutical clinical research experience on clinical trials in biotech, pharmaceutical, or CRO environment.
Experience working on global clinical trials and with clinical trial systems (CTMS, eTMF, EDC).
Proficiency in MS Office tools including Word, Excel, and PowerPoint for data management and documentation.
Experience managing multiple clinical trial activities across study lifecycle including risk management, vendor oversight, and site engagement.
Strong familiarity with global trial operations, clinical data compliance, and regulatory documentation.
Capability to identify operational risks early and escalate with proposed solutions, supporting inspection readiness and process improvements.