SEARCH CAREER OPPORTUNITIES

GENERAL SUMMARY OF POSITION:

SPARC focuses on conducting research and developing knowledge to improve services, quality of life, and promote recovery for people with or at risk of mental health conditions, and their families. A main component of SPARC is the dissemination of knowledge through a range of activities that include teaching, publishing, speaking, consulting, and training.  Adhering to established protocols, the research coordinator will be responsible for recruiting study participants over the telephone, managing study data, collecting and quality-checking data (qualitative and quantitative from participants, providers, and practices), analyzing survey responses, analyzing qualitative data for emerging themes and drafting codebooks. The research coordinator will maintain effective working relationships with study practices to facilitate data collection. The research coordinator will assist in the development of qualitative survey instruments and verify existing measures to be included in a new research project. An individual familiar with REDCap, Quickbase, NVivo and Dedoose for data analyses preferred. The research coordinator will adhere to Good Clinical Practice (GCP) guidelines and all human participant protection practices.

Under the direction of the Principal Investigator or designee, the Research Coordinator I is responsible for carrying out multiple complex research protocols.

This position requires flexibility to work on some night shifts and weekend schedule. 

MAJOR RESPONSIBILITIES:

• Collaborate with investigators in the design, development, and documentation of data forms, questionnaires, and other survey materials
• Responsible for aspects of the development of research recommendations and the design of research projects
• Participate in the grant, manuscript, and Institutional Review Board process
• Develop overall research plan for conducting surveys in the community
• Conduct in-person or telephonic field research
• Monitor selection and randomization process of study participants
• Coordinate data collection of study participants, complete case report forms, and develop and maintain spreadsheets
• Collect and maintain questionnaires and other data forms from study participants
• Perform literature searches and write detailed written summaries of the findings
• Collaborate with other project leaders on data presentation, interpretation and writing of scientific reports 
• Develop and maintain computerized data files for all data to be collected
• May assist with budget /operational aspect of grant and contract proposals
• Prepare summary reports and ongoing project evaluations for investigators
• May help recruit, select, supervise and direct the activities of data collection employees and Research Technicians
• Conduct quality control check on field data collection system
• Collaborate with other research sites to insure consistency between research sites and accuracy of documentation
• Perform other duties as required.

REQUIRED QUALIFICATIONS:

• Bachelor’s degree in the sciences, health care, or equivalent experience
• 1 year of related experience
• Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
• Oral and written communication skills
• Excellent organization, analytical, and interpersonal skills required
• Ability to travel to off-site locations

SUPERVISION RECEIVED:

Under the direction of the Principal Investigator or designee

SUPERVISION EXERCISED:

May supervise and direct the activities of data collection employees and Research Technicians

ENVIRONMENTAL WORKING CONDITIONS:

Usual office environment, laboratory, medical, surgical, and off campus study sites

 This position requires flexibility to work on some night shifts and weekend schedule.