Clinical Research Associate

The University of California, San Diego is a student-centered, research-focused, service-oriented public institution that provides opportunity for all. Recognized as one of the top 15 research universities worldwide, a culture of collaboration sparks discoveries that advance society and drive economic impact.

The Department of Reproductive Medicine is conducting research studies to identify better predictors of poor pregnancy outcomes. Clinical data and biospecimens are being collected at several clinical sites from normal and high-risk pregnancies.

Under supervision, the incumbent will be responsible for recruiting subjects and collecting samples and clinical data for studies in the Department of Reproductive Medicine. Responsibilities include: maintaining relationships with recruitment sources; screening potential research subjects; enrolling appropriate research subjects into clinical research studies; establishing and maintaining methods for recruitment data collection; collecting and processing biospecimens; collecting clinical data. The individual will abstract information from medical records, code and enter data, perform basic data analysis, write preliminary reports, and update databases.

**Minimum Qualification:** * Must be certified in Phlebotomy or willing to undergo training for certification. * Theoretical knowledge in Biological Sciences or related field; or equivalent experience in health services setting. Strong theoretical knowledge in biology, medicine, or related field. * Strong proven written and verbal communication skills and organizational skills. Strong interpersonal skills and ability to communicate with health professionals, patients, and caregivers. * Excellent interpersonal skills, ability to elicit patient cooperation and work in interdisciplinary team harmoniously. * Proven experience using various software packages such as MS Word, PowerPoint, and database such as Excel or Access to prepare various research reports for presentation and data analyses. * Demonstrated attention to detail; ability to keep accurate and complete records. * Demonstrated ability to complete difficult work assignments. Proven ability to work in a fast-paced environment with rapidly changing priorities. * Ability to handle and work with human tissues and other biohazardous, toxic, and carcinogenic materials and to recognize safety problems. * Demonstrated knowledge of radiation safety and biosafety techniques and practices. Ability to follow established Safety and Biohazardous Material Guidelines. **Preferred Qualification:** * Experience in establishing and maintaining relationship with outside agencies and in-house groups to recruit subjects into Clinical Research Studies. * Experience in recruiting research subjects into clinical studies. Knowledge of informed consent issues. **Special Condition:** * Must be available for working according to variable schedules including occasional weekends. * Must be able to work occasional extended shifts and/or flexible hours. * Must have a valid California driver's license and/or reliable transportation. * Must be able and willing to travel off-site.