Clinical Research Coordinator (SRA II)

Location: 
4150 Clement St
San Francisco, CA 94121
United States
Job Posted Date: 
March 9, 2021
Opportunities: 
Full-time Positions
Population: 
Medicine

The incumbent will serve as the Study Coordinator for the research project and will provide day-to-day study coordination activities for research studies involving opioid dependence.

 

Job Responsibilities:

  • Create study protocol, consent forms and all other materials requiring IRB approval
  • Obtain all UCSF, VA and other regulatory approvals required to begin and continue study operations
  • Coordinate the daily study operations
  • Work closely with Investigators to develop and modify the protocol and ensure all Investigators are trained on protocol
  • Coordinate with NCIRE Contracts and Grants staff  and other study team members to meet regulatory and sponsor reporting
  • Serve as the primary contact for the study
  • Oversee systems for tracking / monitoring study progress to ensure adherence to timelines, SOPs, and applicable regulations
  • Maintain essential research study documentation 
  • Work closely with the project manager to develop recruitment strategy and materials, and ensure adherence to the enrollment goals of the study  
  • Recruit participants for the study
  • Responsible for providing and documenting Informed Consent
  • Schedule all assessment study visits  and study procedures
  • Maintain rapport with study participants
  • Assist Program Manager with preparation of progress reports for funding agencies
  • Perform other duties as assigned
  • Conduct study assessment surveys and qualitative interviews with participants. 
  • Participate in basic quantitative and qualitative data analysis. 
Job Requirements: 
  • Minimum of 1 year research experience, with direct human research study management, and experience in managing IRB protocols
  • Experience in coordinating research studies, preferably in a VA setting
  • BA degree in health science or related fields preferred
  • Has a thorough understanding of FDA, ICH, and GCP regulations, guidelines, policies and practices for conducting clinical investigations
  • Computer literacy with emphasis on Windows operating systems and software applications
  • Excellent interpersonal, written/oral communication and organizational skills
  • Ability to manage multiple projects, tasks and priorities to achieve desired goals
  • Strong accuracy and attention to detail
  • Ability to work under minimal supervision
How to Apply: 

For more information about Northern California Institute for Research and Education (NCIRE) or to apply for this exciting opportunity, please visit us at www.ncire.org.

 

Please directly apply by cutting and pasting the below link into your browser. Any applications submitted through this job website will not be considered. All interested candidates must only apply using the link below to be considered.

 

https://recruiting.ultipro.com/NOR1032NCIRE/JobBoard/ae6d11d3-2f59-4e1f-8104-cb70bc41b619/Opportunity/OpportunityDetail?opportunityId=014a4b50-c1d8-46df-9280-3ec2dfda61a5

 

Northern California Institute for Research and Education (NCIRE) is proud to be an Equal Opportunity Employer.

•     Per San Francisco's Fair Chance Ordinance, Northern California Institute for Research and Education (NCIRE) will consider qualified applicants with criminal histories

•     Principals only. Recruiters, please don't contact this job poster.

Location: 
San Francisco
Greater Bay Area
Peninsula
California