Clinical Research Project Manager

Responsibilities

• Develop and execute detailed project plans, timelines, and budgets in collaboration with principal investigators.
• Manage a cluster randomized trial involving high-risk women and primary care providers, monitoring recruitment and data collection.
• Collect and analyze quantitative and qualitative data related to chemoprevention uptake and decision-making.
• Conduct equity-focused evaluations using the Consolidated Framework for Implementation Research (CFIR).
• Prepare progress reports, manuscripts for scientific journals, and presentations for conferences.
• Coordinate IRB compliance, including renewals, modifications, and annual progress reports.
• Assist with project finances, including managing external vendor invoices and payments.
• Participate in human-centered design activities, including usability testing and prototype evaluations for decision support tools.

Requirements

• Bachelor's degree or equivalent in education and experience.
• 3 years of related work experience.
• Proficiency with MS Word and familiarity with Mac and PC platforms.
• HIPAA training certification.
• Good Clinical Practice (GCP) certificate.
• Conflict of Interest (COI) training certification.
• Excellent written and interpersonal communication, analytical, and organizational skills.

Preferred Qualifications

• Master’s degree or equivalent with 1 year of relevant experience in research.
• Managerial skills to oversee and train part-time staff and research personnel.
• Knowledge of statistical software packages and qualitative research methodologies.

About the Company

The Department of Biomedical Informatics at Columbia University is conducting NCI-funded research focused on informatics-driven breast cancer prevention and decision-support tools.