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Assistant Research Coordinator

Rutgers Biomedical and Health Sciences
New Brunswick, USA
Full-time
Entry · 2+ years experience
Hybrid
USD 58953-83479 yearly / year
Discovered 1 months ago
REDCap

Full Job Posting

Posting Summary

Recruits, consents, schedules and interviews study subjects.

Collects quantitative and qualitative data from subjects and/or medical records.

Creates and manages documents for Institutional Review Board ( IRB ) and other study related activities.

Prepares protocols, informed consent documents, modifications, renewals and other necessary documents for review by the IRB and/or sponsor.

Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis.

Keeps neat, thorough, and up-to-date records of procedures and analyses, using paper and electronic platforms.

Timely and accurate entry of data into research databases. Regularly audits database for errors and obtains missing information.

Benefits

  • Medical, prescription drug, and dental coverage
  • Paid vacation, holidays, and various leave programs
  • Competitive retirement benefits, including defined contribution plans and voluntary tax-deferred savings options
  • Employee and dependent educational benefits (when applicable)
  • Life insurance coverage
  • Employee discount programs

Minimum Education and Experience

Bachelor’s Degree in a relevant science plus two (2) years experience.

Required Knowledge, Skills, and Abilities

  • Proficiency with Internet applications and in using various Microsoft Office applications such as Word, Excel, Power Point and Outlook, online search engines and fluency with learning new software applications.
  • Ability to manage multiple research projects simultaneously with high degree of accuracy and attention to detail.
  • Excellent interpersonal, organizational, communication (oral and written), and problem-solving skills.
  • Ability to interface effectively with all levels of management. Must work and communicate effectively with both internal and external team members. Demonstrates flexibility to work in a collaborative environment.
  • Strong organizational and time management skills and ability to multitask and work well under pressure to meet time deadlines.
  • Self-starter who is detail oriented, analytical, has strong organizational skills and the ability to work independently.
  • Ability to identify, analyze and solve problems.
  • Be highly motivated to obtain knowledge on project-related research topics.

Preferred Qualifications

  • Master’s Degree preferred. .
  • Experience with human subjects research and/or patient interaction in a clinical setting, preferred.
  • Experience with Institutional Review Board ( IRB ) submission and manuscript preparation strongly preferred.
  • Experience with grant writing and budgeting, preferred.
  • Interest in in-hospital cardiac arrest, social emergency medicine, and ultrasound, preferred.
  • Experience with REDCap database software and implementing REDCap surveys and databases, preferred.
  • Fluency in Spanish preferred.

Physical Demands and Work Environment

Physical Demands: Reading, standing, sitting, walking, talking and hearing. Lifting up to 25 lbs.

Work Environment: Office environment with moderate noise.

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