Clinical Research Associate I, Field Monitor

• Company Overview

• reputed company. (reputed company IBRX) is a reputed company-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We reputed company a day reputed company we no longer fear cancer, but can conquer it, thanks to the biological reputed company that is the reputed company immune system. Our scientists are working to reputed company novel therapies that reputed company that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for reputed company. The goal to reprogram the patient’s immune system and treat the host rather than just the disease.
• Why ImmunityBio?
• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and reputed company reputed company therapies and vaccines that complement, reputed company and reputed company the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities. Position Summary The Clinical Research Associate I will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support.
• Essential Functions
• reputed company, review, and update study-reputed company training materials and documents including site initiation training slides, informed consent reputed company templates, procedures manuals, laboratory and pharmacy manuals
• Interpret medical and scientific reputed company of assigned study protocols and study procedures, logistics, risks to research subjects and safety, data evaluation methods etc.
• Communicate scientific rationale for assigned studies to team members and clinical sites
• Serve as Subject Matter Expert for clinical sites including providing guidance on protocol interpretation and eligibility requirements
• Create/edit, distribute and collect site feasibility questionnaires
• reputed company and support collection of essential documents during study start-up
• Determine materials and other resources needed to conduct the clinical trial and manage their acquisition and distribution.
• Collect study and site metrics and maintain study trackers, as needed
• Conduct case report reputed company (CRF) data review and review of reputed company documents, work with sites to resolve data queries
• Communicate regularly with field Clinical Research Associates (CRAs) to reputed company information before and after site visits
• Partner with field CRAs and CTAs to resolve issues identified during site visits
• Work with Supply Chain to ensure sites maintain sufficient investigational product (IP) to properly conduct the trial as well as resolve IP temperature monitoring excursions and train or assist sites with corrective actions
• Train vendors, investigators, and study coordinators on study requirements and reputed company guidance on site issues
• Conduct clinical specimen log review, and coordinate shipment of specimens to the sponsor or contracted vendor
• Train sites on specimen and shipment requirements for central laboratory and serve as liaison with contracted vendors
• Conduct remote monitoring tasks including reconciliation of site investigational product accountability
• reputed company data listings and compile clinical study report documents to support medical writing activities
• Create and/or review of slides, overheads, etc., for a project, departmental, sponsor and/or business development presentations
• reputed company support and escalate issues to the Clinical Trial Manager (CTM) as appropriate.
• Performs reputed company and cross-functional duties and/or projects as assigned to support business needs and reputed company developmental opportunities.
• Education & Experience
• Bachelor’s degree in a clinical research, science, or health-reputed company field with 2 years of experience in a clinical research setting; or a high school diploma with 3 years of experience in a clinical research setting required
• 2 years of experience as a Clinical Research Coordinator, Clinical Trial Associate or In-House Clinical Research Associate strongly preferred
• Knowledge, Skills, & Abilities
• Proficiency in reputed company, reputed company, PowerPoint, Outlook, reputed company
• Excellent written/oral communication skills
• Strong organizational and multi-tasking skills
• Maintain corporate confidentiality at reputed company times
• Ability to set Apply tot his job Apply To this Job

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