Clinical Research Associate - Oncology at ODC Pharma | Torre
Clinical Research Associate - Oncology
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ODC Pharma

Clinical Research Associate - Oncology

ODC Pharma
Posted by
Stephanie Moore
Emma
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Freelance
Recurrent
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Remote (for United States residents)
Remote (for Canada residents)
Posted 8 months ago

Responsibilities

- Must have experience monitoring in Oncology. - Bachelor’s degree in life sciences or health-related field (or equivalent experience). - Responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. - Conduct all types of site visits—selection, initiation, monitoring, and close-out—in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. - Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals. - Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity. - Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries. - Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
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