University of California San Diego
Location
La Jolla, CA | United States
Job description
UCSD Layoff from Career Appointment : Apply by 03/01/2024 for consideration with preference for rehire. All layoff applicants should contact their Employment Advisor.
Special Selection Applicants : Apply by 03/12/2024. Eligible Special Selection clients should contact their Disability Counselor for assistance.
The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
Reporting directly to the Translational Project and Lab Manager, the Translational Research Coordinator I supports the clinical research efforts of the MCC by providing comprehensive coordination and data management for a portfolio of translational research protocols.
The incumbent is responsible for supporting and coordinating translational research protocols, including recruitment, consenting, research chart preparation, data collection and record-keeping, and ensuring all protocol requirements are met. Assure compliance with state and federal regulatory guidelines. Assist in ensuring the quality of the medical and clinical research data. Assist in providing guidance to investigators. Provide education and information to the general public concerning the ongoing clinical trials. Assist PIs with proposals, progress reports and manuscripts. Under direct supervision, create original documents and policies for assigned disease teams. Work closely with federal and state regulatory officials.
Theoretical knowledge and/or Bachelor's Degree in social science, biological sciences, or a related field, and/or an equivalent combination of education and experience.
Demonstrated advanced organizational and project management skills (preferably in an academic setting), including the ability to work independently, determine priorities, complete multiple projects accurately, efficiently, and with a high level of attention to detail while working with conflicting deadlines.
Experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Experience handling, transporting, and/or processing biospecimens such as blood, tissue, and urine.
Experience in research protocol start-up procedures, including: study feasibility, study activation and IRB processes, and qualification procedures. Experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement.
Excellent written skills and knowledge of the English language, including grammar, spelling, and punctuation usage. Ability to compose, edit, and finalize correspondence.
Interpersonal skills with strong, demonstrated ability to communicate orally and in writing. Possess skills of tact, poise, diplomacy, confidentiality, and flexibility. Ability and willingness to work independently and/or in a team framework in conjunction with principles of community and with a diverse population of staff, faculty, and members of the community.
Ability to demonstrate a high degree of professionalism in a rapidly changing, time-pressured environment. Independent judgment, strong organizational skills, and the ability to be flexible as demands and priorities change.
Working knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation). Working knowledge of medical and scientific terminology.
Knowledge of experimental protocols, data gathering, protocol design and evaluation.
Ability to maintain confidentiality.
Experience in clinical trials research.
Demonstrated experience in research protocol procedures, design, monitoring, Human Subject Rights, and informed consent procedures.
Experience with laboratory procedures and values and experience interpreting them to determine patient eligibility and potential toxicities.
Computer proficiency, including working knowledge of word processing, spreadsheet software (Microsoft Office) and internet browser applications. Experience conducting searches on the internet.
Bachelor's degree in related area and / or equivalent experience / training.
Certification as a Clinical Research Associate or Coordinator.
Experience completing clinical trials case report forms via hard copy and online.
Enthusiasm for learning and a genuine interest in scientific research. Willingness and ability to learn new skills,
About University of California San Diego
UC San Diego is an academic powerhouse and economic engine, recognized as one of the top 8 public universities by U.S. News and World Report. Innovation is central to who we are and what we do. Here, students learn that knowledge isn't just acquired in the classroom - life is their laboratory. UC San Diego's rich academic portfolio includes six undergraduate colleges, five academic divisions and five graduate and professional schools. The university's award-winning scholars are experts at the forefront of their fields with an impressive track record for achieving scientific, medical and technological breakthroughs.
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