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Remote option, metro location, and reputable CRO brand increase applicant density.
Clinical trials and regulatory expertise make skills highly industry-specific and less transferable.
Explicit 9+ years and 4+ years study-lead requirements plus regulatory and vendor management mandates.
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Manage and oversee data management activities across one or more clinical trials ensuring alignment with study objectives and compliance with regulatory standards.
Maintain inspection readiness and support internal and regulatory audits throughout the trial lifecycle.
Lead planning, execution, and delivery of key data management deliverables while providing team leadership and cross-functional collaboration.
Bachelor’s degree in Life Sciences, Health Sciences, or related discipline.
9+ years of clinical data management experience including hands-on clinical trial involvement.
Minimum 4+ years of experience as a Study Lead managing clinical studies independently.
Proven knowledge of clinical data management processes, systems, and global regulatory requirements.
Experienced in operating within global, cross-functional, and multicultural clinical trial environments.
Demonstrated leadership and project management skills with a track record of managing vendors and complex deliverables.
Strong proficiency in data analysis and communication of clinical data insights to diverse stakeholders.