GENERAL SUMMARY OF POSITION:

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

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

Applicants must be comfortable approaching patients in the ED and acute care setting.

PREFERRED QUALIFICATIONS:

• Experience in healthcare setting, either clinical or research
• The applicant will be working on multiple projects so flexibility is a must
• Off-site travel will be required to UMass Memorial Community EDs
• Excellent interpersonal skills to interact with a diverse array of research participants, physicians, clinical staff, and other members of the research team
• Basic computer proficiency (Word, Excel, email)