University of California, San Francisco→
Assistant Clinical Research Coordinator at University of… · San…
Entry LevelOn-siteFull-timeSan Francisco, CA
Skills
human subjects researchdata collectionproject managementmicrosoft office suiteredcapanalytical skillscommunication skillsinterpersonal skillsorganizational skillsproblem-solving skills
Job Description
Summary: The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research. The Assistant Clinical Research Coordinator will support the coordination of clinical studies focused on mindfulness-based and lifestyle behavior interventions for people living with systemic autoimmune rheumatic diseases, assisting in various administrative and research coordination tasks.
Responsibilities:
- Perform entry-level duties related to the support and coordination of clinical studies
- Assist in the coordination of one or more single or multi-site, active or follow-up clinical trials
- Help prepare protocols for study initiation
- Design flow sheets, data forms and source documents
- Gather and interpret medical, surgical and laboratory data regarding clinical trial subjects
- Apply understanding of inclusion/exclusion eligibility criteria for protocols
- Help recruit, enroll, register, schedule and retain study subjects
- Record protocol specific treatments and assure collection and shipment of samples
- Assist research personnel to keep patients on study schedules
- Complete study forms to submit to sponsors and/or appropriate agencies
- Collect, enter and clean data into study databases, maintaining data quality
- Assist with preparation of reports and tables
- Attend team meetings
- Perform other duties as assigned
- Assist the PI and other staff in recruiting, screening, enrolling, tracking and follow-up of participants
- Collecting and entering study data
- Work closely with Dr. Patterson to ensure seamless program coordination and data collection and management
- Assist with data organization and basic data analyses
- Adhere to study guidelines
- Keep accurate records
- Maintain confidentiality
- Attend regular study team meetings
- Complete study forms and evaluations and other duties as assigned
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, PowerPoint, Excel, box.com, and REDCap
- 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 study participants, investigators, and co-workers
Preferred Qualifications:
- Experience working in human subjects research
- Experience working with patients with chronic illness, in either a clinical or research setting
Required Skills: Human subjects research, Data collection, Project management
Important Skills: Microsoft Office Suite, REDCap
Nice-to-Have Skills: Analytical skills, communication skills, Interpersonal skills, Organizational skills, Problem-solving skills