Elephas
Elephas is developing an ex-vivo technology suite to assess how live tumor fragments (LTFs) respond to immunotherapies. We seek to remove the trial-and-error approach to cancer care by harnessing the latest advances in cancer biology, advanced imaging, and artificial intelligence to accelerate drug development and empower clinical decision-making. Our unique approach maintains the native 3-dimensional cellular architecture and micro-environment of the tumor, enabling rapid real-time characterization of live tumor sample response to immunotherapies.
51 - 200 employees
Clinical Research Associate
February 15
Elephas
Elephas is developing an ex-vivo technology suite to assess how live tumor fragments (LTFs) respond to immunotherapies. We seek to remove the trial-and-error approach to cancer care by harnessing the latest advances in cancer biology, advanced imaging, and artificial intelligence to accelerate drug development and empower clinical decision-making. Our unique approach maintains the native 3-dimensional cellular architecture and micro-environment of the tumor, enabling rapid real-time characterization of live tumor sample response to immunotherapies.
51 - 200 employees
📋 Description
• The Clinical Research Associate (CRA) is responsible for monitoring clinical study sites during study start-up, study recruitment, and follow-up and close out study phases. • The CRA will support site initiation visits, platform/process training, clinical education, sample collection oversight, implementation of subject recruitment strategies, and communicating with appropriate site staff and investigators for the successful completion of studies. • This role will be responsible for site-related KPIs for data entry, including data completion, query resolution and data validity. • Travel is expected to be up to 50% for this position. • Administer protocol and study related training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluates the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. • Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
🎯 Requirements
• Bachelor’s Degree required • Bachelor’s Degree in a scientific or healthcare-related field highly preferred • Minimum of 2 years of experience as a Clinical Research Associate • Previous on-site monitoring experience required • Minimum of 5 years in the clinical research industry at the site, sponsor or CRO level • In-depth knowledge of oncology clinical trials, specifically solid tumors
🏖️ Benefits
• competitive compensation and benefits • paid time off • health insurance • life insurance • flexible spending accounts • a 401(k) plan • stock options
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🇺🇸 United States – Remote
💵 $140k - $175k / year
💰 $10M Seed Round on 2016-12
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
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