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Tier-1 employer and metro location increase applicant density.
Clinical trial operations are highly industry-specific to biotech/pharma/CROs.
Explicit regulated clinical experience and domain-specific skills make screening stringent.
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Provide global study management support to clinical study teams focusing on start-up and execution activities ensuring timely and compliant delivery.
Own specific study tasks including study-level tracking, vendor management, risk monitoring, and issue escalation with proposed solutions.
Coordinate site and vendor engagement, maintain clinical trial systems, and contribute to process improvements and audit readiness.
Bachelor’s degree with 2 years clinical execution experience OR Associate’s degree with 6 years clinical execution experience OR High school diploma/GED with 8 years clinical execution experience.
At least 3 years work experience in life sciences or medically related field, including 1 year in biopharmaceutical clinical research in biotech, pharma, or CRO, with global clinical trial exposure.
Proficiency in clinical trial systems such as CTMS, eTMF, EDC, and MS Office tools.
Not explicitly mentioned: notice period or location constraints.
Experienced in clinical trial operations and oversight within biotech, pharmaceutical, or CRO environments with strong process and compliance focus.
Skilled in managing vendor relationships, risk-based monitoring, audit/inspection readiness, and corrective/preventive actions (CAPA).
Effective in cross-functional global collaboration with strong communication and issue escalation capabilities.