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Yale University

Research university in New Haven, CT

Research Project Manager

Full-Time
$65k - $101k
Junior
Master's
New Haven, CT, USA
In PersonOn-site.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • Demonstrated proficiency in managing diabetes-related technological devices, including continuous glucose monitoring, wearable devices, and ecological momentary assessment.
  • Demonstrated proficiency in project management, including budgeting, planning, execution, delivery, quality assurance, and reporting.
  • Related experience in a health-related field such as public health, nursing, psychology, or health policy, including working with confidential data and maintaining confidentiality, privacy, and integrity.
  • Exceptional attention to detail and organizational, communication, and interpersonal skills; ability to work independently and balance multiple projects and tasks simultaneously.
  • Ability to work as a member of and effectively and proactively lead teams; comfort in a clinical environment, including ability to interact with patients.
  • A master's degree in a related discipline and two years of experience, or an equivalent combination of education and experience.
  • Meet healthcare-worker health requirements before starting work, including MMR and varicella vaccination or immunity, TB screening, COVID vaccination according to University policy, hepatitis B vaccination or immunity, and annual flu vaccination.
  • Successfully complete the required pre-employment background screening, which may include motor vehicle, DOT certification, drug testing, and credit checks based on the position description and job requirements.
Responsibilities
  • Carry out research within the scope of the established study protocol and adhere to human-subjects regulations defined by Yale University and the federal government.
  • Develop criteria for admission of study subjects based on project goals and objectives.
  • Determine potential sources of funding and prospective partnerships.
  • Evaluate the feasibility of potential projects by analyzing staffing needs, resource requirements, financial costs, and current group capacity; negotiate contracts or changes with funders.
  • Develop original HIC/IRB submissions; collaborate with principal investigators on major revisions and scientific protocols; plan and implement changes.
  • Develop forms, questionnaires, and research techniques, and write procedure manuals for data collection and coding.
  • Document and transmit study data, ensuring report forms are accurately completed and submitted on time at each site.
  • Independently develop, manage, and organize multi-site studies; coordinate between the University, non-Yale collaborators, pharmaceutical companies, HIC, IRB, and funding sources.
  • Perform descriptive and multivariate statistical analyses of data using computer software.
  • Design and implement quality-control measures to ensure accurate data collection and processing.
  • Contribute original analysis and relevance to written reports and help write abstracts and manuscripts.
  • Manage clinical research projects, including patient recruitment, data collection, protocol compliance, data management, and preparation of reports and publications.
Desired Qualifications
  • Experience preparing IRB protocols, amendments, and progress reports.
  • Experience with clinical trials, including patient recruitment and regulatory submissions.
  • Experience with database management, including Microsoft Access; REDCap experience is preferred, as is experience with statistical analysis software.
  • Prior experience working on large-scale research studies or multi-visit projects.

About the company

Yale University is a private research university in New Haven, Connecticut. It provides undergraduate, graduate, and professional education alongside research, scholarship, and public engagement.

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