Position available through UCSD Temporary Employment Services (TES). Employment through TES is an excellent way to gain valuable UCSD experience and get your foot in the door for career positions. TES employment includes medical coverage, paid vacation & sick time, paid holidays, as well as training and development opportunities!
The Clinical Research Coordinator is responsible for coordinating clinical trials, such as screening for patient eligibility, data collection, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files. Assist the department with human subjects submissions, renewals, and safety reports.
Directly communicate with assigned physicians and disease groups, including attending meetings when requested. Provide direct assistance to the Patient Care Coordinator in reviewing, verifying and maintaining university research account statements, bulk accounts, VELOS, EPIC, script logs and Departmental Research Agreements, sponsor invoicing and any additional tasks.
Certified Clinical Research Coordinator.
Theoretical knowledge of biology, microbiology, social sciences, or related field.
Demonstrated experience performing clinical research duties in a clinical research environment.
Proven experience interpreting medical charts, experience in abstracting data from medical records.
Demonstrated experience working with investigational drug authorization criteria.
Experience using statistical software applications. Knowledge of database, word processing and spreadsheet applications such as CREDIT, Access, Excel and MS Word.
Experience with laboratory procedures and values and experience in interpreting them to determine patient eligibility and potential toxicities.
Experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Experience in medical assessment and patient interviewing to determine toxicities related to protocol management.
Demonstrated experience completing clinical trials case report forms via hard copy and online.
Excellent communication skills, both oral and written using grammatically correct English.
Solid interpersonal skills, including tact, diplomacy, and flexibility. Ability to interact effectively with diverse groups, including professional and non-professional staff and clients.
Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately.
Ability to work independently. Ability to maintain confidentiality.
A background check is required.
Must to be open to non-standard work hours.
The University of California is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, age, protected veteran status, gender identity or sexual orientation. For the complete University of California nondiscrimination and affirmative action policy see: http://www-hr.ucsd.edu/saa/nondiscr.html
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University Of California