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Tier-1 employer and metro location increase applicant density, but clinical trial specialization limits broad applicant pool.
Clinical trial operations require biotech/pharma domain knowledge and systems, limiting transferability across industries.
Explicit education/experience alternatives plus required clinical systems, regulatory and vendor expertise make screening strict.
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Provide global study management support ensuring timely, high-quality, and compliant clinical study execution.
Own specific study tasks including study planning, coordination, risk monitoring, and issue management, escalating early warnings with solutions.
Maintain study trackers, dashboards and coordinate logistics while engaging stakeholders, vendors and study teams to monitor progress and compliance.
Minimum education: Master’s degree OR Bachelor’s with 2 years clinical execution experience OR Associate’s with 6 years clinical execution experience OR High school diploma with 8 years clinical execution experience.
Work Experience Required: 3 years in life sciences or medically related field including 1 year in biopharmaceutical clinical research with clinical trials exposure at biotech, pharma, or CRO.
Experience working on global clinical trials and managing vendors/suppliers.
Proficient with clinical trial systems such as CTMS, eTMF, EDC and Microsoft Office tools.
Experienced in biotech, pharmaceutical, or CRO environments supporting global clinical trial operations and oversight.
Skilled in risk-based site monitoring, audit readiness, CAPA processes, and ensuring regulatory compliance.
Capable of managing complex clinical data flow and documentation to ensure inspection readiness and streamlined study execution.