San Diego Supercomputer Center · 11 hours ago
Clinical Research Assistant/Interviewer - French - 138207
San Diego, CA
Full-time
Onsite
New Grad, Entry Level
$33.57/hr - $54.01/hrThe San Diego Supercomputer Center is seeking a Clinical Research Assistant/Interviewer who will be responsible for coordinating and managing multi-site prospective pregnancy registry studies. The role involves patient recruitment, data collection, and ensuring protocol compliance while requiring fluency in both English and French.
Big DataDatabaseInformation Technology
Responsibilities
Coordinating and managing multi-site prospective pregnancy registry studies
Providing all aspects of protocol management
Screening for patient eligibility
Data collection and analysis
Ensuring protocol compliance
Adverse drug reaction reports
Maintenance of accurate and complete clinical research files
Recruitment and follow-up of pregnant women who take certain medications and vaccines
Comparison pregnant women without these exposures
Recruit, interview, and follow up with participants who are monolingual French speakers
Ensuring accurate communication of study information and sensitive health-related topics
Promote the project at scientific and professional meetings
Distribute study materials to clinics in San Diego County
Perform other duties as assigned
Qualification
Required
Theoretical knowledge of biology, microbiology, social sciences, clinical sciences as typically attained by a Bachelor's degree, or an equivalent combination of education and experience
Must be fluent in English and French, preferably Canadian French
Experience performing clinical research duties in a clinical research environment
Experience using database, word processing and spreadsheet applications such as Velos, Access, Excel and MS Word
Experience with laboratory procedures and values and experience in interpreting them to determine patient eligibility and potential toxicities
Experience working with FDA policies regulating clinical trials
Experience in medical assessment and patient interviewing to determine toxicities related to protocol management
Experience interpreting medical charts, experience in abstracting data from medical records
Experience with clinical trials participant or study subject recruitment
Experience coordinating study startup activities
Experience providing in-service training to various research personnel on protocols, processes, and procedures
Knowledge of x-rays, scans, and other diagnostic procedures
Experience maintaining files and keeping records
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
Excellent interpersonal, as well as written and verbal communication skills (using grammatically correct written English and accurate typing) to interact with a diverse population. Excellent phone etiquette skills
Ability to work independently. Ability to maintain confidentiality
Experience completing clinical trials case report forms via hard copy and online
Demonstrated ability to interact effectively with diverse groups, including professional and non-professional staff and clients
Preferred
Certification as a Clinical Research Associate or Coordinator
Experience working with research bulk accounts
Experience with investigational drug authorization criteria
Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource Protection Program (HRPP), IATA Shipping of Blood Specimens, and Bloodborne Pathogens
Company
San Diego Supercomputer Center
SDSC enables science and engineering discoveries through advances in computational science and data-intensive, high-performance computing.
Founded in 1985
201-500 employees
Funding
Current Stage
Growth StageTotal Funding
unknownKey Investors
National Science Foundation
2024-12-05Grant
Leadership Team
Ilkay Altintas
Division Director, Cyberinfrastructure and Convergence Research and Education
Recent News
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