Job Description

South San Francisco, CA


Contract Duration: 12 months


Rate: Negotiable


Salary: NA, $1.00

• Excellent employment opportunity for a Clinical Research Associate in the South San Francisco area.
• Assists in the selection of investigational sites, negotiates grant contracts with each, and conducts site training for the study
• Assists in the setting and updating study timelines.
• Attends study management team meetings
• Assists in CRO or vendor selection and management of vendors.
• May assist in the review of protocols, informed consents, case report forms, monitoring plans, or clinical study reports.
• Assists in the review of routine data and resolution of data discrepancies.
• Interfaces with individuals in other functional areas to address routine study issues.
• May be asked to assist in the training of Clinical Trial Assistants.
• May conduct site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required.
• Assures site compliance with the routine protocol and regulatory requirements and quality of data.
• May resolve routine monitoring issues.
• May perform site monitoring to assure protocol and regulatory compliance, and the timely submission of complete and accurate study data forms
• Monitors case report forms, identifying and resolving discrepancies
• Tracks clinical trial documentation and retrieve, process and tabulate clinical or study compliance data to ensure smooth initiation, operation and timely completion of the clinical trial
• Must be current and up to date with required company SOPs and trainings at all times
• Must be current and up to date with industry regulations
• Phase I II Oncology experience

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