Job Description

The UCSF Airway Clinical Research Center (ACRC) integrates research programs in asthma, COPD, sarcoidosis, and cystic fibrosis, along with current programs sponsored by the National Institutes of Health and the pharmaceutical industry. Reporting to and under the direct supervision of the Research Manager, the incumbent will perform entry-level duties related to the support and coordination of clinical studies, including the SPIROMICS/SOURCE studies and American Lung Association (ALA) network studies. The incumbent may receive training and development to prepare and advance for journey-level work at the next level within the series. The Asst. CRC's major responsibilities include training and learning how to screen and schedule research subjects, assist research personnel to keep patients on study schedules; learning how to collect, enter and clean data into study databases, maintain data quality; assist with preparation of reports and tables; attend team meetings; and perform other duties as assigned.

Qualifications

Required Qualifications:

• HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
• Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.
• Proficiency with Microsoft Word, Excel, PowerPoint, and Windows.
• Excellent analytical and problem-solving skills.
• Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
• Ability to establish cooperative working relationships with research subjects, co-workers, & physicians.

Preferred Qualifications:

• Proven and demonstrated experience in various social media platforms, including Facebook, Twitter, Instagram, YouTube
• Proven and demonstrated experience in updating and maintaining product content and design elements
• Experience working with patients or study subjects
• Prior experience in clinical trial recruitment
• Proficiency working with medical records and abstracting data for evaluation of recruitment feasibility and/or progress.

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