Research Coordinator

3 weeks ago

Philadelphia, Pennsylvania, United States Drexel University Full time
Job Summary

Under the supervision of the Principal Investigator (PI) and in close collaboration with other study investigators, personnel, and students, this full-time Study Coordinator/Organizational Coach will be responsible for coordinating all aspects of an NIH-funded trial aimed at increasing organizations' use of best practices in HIV prevention programming in up to 32 syringe service programs (SSPs) across the United States.

Key Responsibilities
  • Assisting with the development and management of data collection systems and study protocols
  • Overseeing recruitment and retention of SSPs
  • Contributing to various aspects of data collection and management
  • Attending regular study meetings
  • Participating in data analysis and dissemination activities
  • Administrative tasks as needed
  • Helping to train and supervise students and/or staff working on related projects
Organizational Coaching Duties
  • With training and support from the study team, working with SSPs to support their implementation of best practices in HIV prevention programming
  • These coaching activities will be conducted remotely (e.g., by video conferencing) and in person, requiring the willingness and ability to travel independently via ground/air (on average, approximately 30% time) and manage work at multiple sites effectively, meet multiple deadlines, and prioritize and organize tasks
Requirements
  • A bachelor's degree in social work, psychology, public health, nursing, or a related field
  • 1-2 years of relevant experience
  • Theoretical understanding and practical knowledge of public health programs and research designs, including experimental/interventional studies, and appropriate evaluation methods
  • Demonstrated experience with research and project coordination on social and/or behavioral science research studies in public health
  • Demonstrated experience in research data collection and quality control
  • Experience with data entry, including knowledge of database, word processing, and spreadsheet applications (e.g., REDCap, MS Word, Excel)
  • Experience maintaining files and keeping research records
  • Excellent written, verbal, and interpersonal communication skills, including tact, diplomacy, and flexibility
  • Demonstrated ability to interact effectively with diverse groups, including co-workers, supervisors, investigators, community collaborators, and study participants
  • Excellent planning and organizational skills and ability to work in a changing, multiple demand setting
  • Demonstrated experience and ability to prioritize a large volume of work and meeting deadlines effectively and accurately
  • Demonstrated skill in problem-solving, critical thinking, attention to detail, and ability to work independently
  • Ability to work effectively as a member of a diverse, multisite research team
  • Thorough knowledge of protocol and goals of studies
  • Experience with SSPs or related community-based or national harm reduction or drug policy-focused organizations

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