Remote Cancer Committee & Protocol Analyst II

University of California - San Diego Medical Centers; San Diego (CA); Hybride; USD 70 000 - 90 000; Plein temps

Résumé du poste

University of California - San Diego Medical Centers (Moores Cancer Center) is seeking a detail-oriented Analyst II to support PRMS review coordination, maintain committee rosters, assign reviewers, and produce agendas and minutes for the Protocol Review and Monitoring Committee. The role involves compiling reports and ensuring precise documentation to advance MCC research initiatives.

Candidates should have extensive experience in clinical research administration, familiarity with NCI/FDA

Qualifications

• Six years of related experience, education/training, OR a Bachelor's degree in related area plus two years of related experience/training.
• Independence, planning and decision-making abilities to complete assigned duties.
• Knowledge of relevant Federal and State regulations, and policies. Ability to interpret NCI requirements for PRMS review and address requirements through supporting committee reviews.
• Ability to solve problems, issues; listen, interpret and confirm understanding of others' communications; and be objective.
• Effective, efficient and tactful oral and written communication skills.
• Time management skills and the flexibility to accommodate changing priorities in unit.
• Ability to work in a team oriented setting, to prioritize work, and to follow through on routine assignments with minimal direction.
• Proficiency with computers, including the ability to operate personal computer software with sophisticated retrieval, storage, and merging capabilities.
• Excellent customer service skills, pleasant, helpful and patient.
• Strong organizational skills, the ability to multi-task, and work with frequent interruptions.
• Human subjects research experience: academic training in the biological or social sciences, humanities or bioethics.
• Experience in research, information evaluation, and the preparation of concise, well-organized reports, summaries, and correspondence.
• Demonstrated ability to collaborate to gather and track key information related to PRMS submissions and study oversight.
• Experience developing and maintaining record management systems. Experience and ability to accurately collect, record, transcribe and synthesize clinical data.
• Knowledge of technical programs supporting recording, videotaping, and remote-meeting access, similar to Zoom and MS Teams.
• Knowledge of investigational protocols (various trial products, data gathering, phases and protocol designs). Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research.
• Demonstrated experience working in a clinical research environment such as CRO, academic research institution, and/or a research hospital. Experience reading and interpreting clinical trials research protocols. Administrative experience in summarizing protocol reviews, ability to format and edit minutes for the Protocol Review and Monitoring Committee.
• Administrative experience using standard word processing and data management software programs, including Word and Excel, to develop and prepare reports. Computer proficiency, including working knowledge of various software programs (such as Adobe Acrobat, web browsers, CTMS, Epic, REDCap, etc.) and internet browser applications. Experience in conducting searches on the internet. Ability and willingness to learn new software as needed.

Responsabilités

• Coordinate and administer PRMS reviews and prioritization by MCC disease teams and Protocol Review and Monitoring Committee.
• Maintain up-to-date membership rosters, assign reviewers to protocols, and coordinate the review process.
• Produce meeting agendas and minutes to record critical outcomes, and generate reports and approval documents.
• Collaborate with committee members and stakeholders to support PRMS submissions, study oversight and documentation.

Formation

Bachelor's degree in related area

Outils

CTMS

Epic

REDCap

Adobe Acrobat

MS Teams

Description du poste

University of California - San Diego Medical Centers (Moores Cancer Center) is seeking a detail-oriented Analyst II to support PRMS review coordination, maintain committee rosters, assign reviewers, and produce agendas and minutes for the Protocol Review and Monitoring Committee. The role involves compiling reports and ensuring precise documentation to advance MCC research initiatives.

Candidates should have extensive experience in clinical research administration, familiarity with NCI/FDA