Sr Clinical Research Coordinator 2
Core
Independently manages the collection, documentation, analysis of clinical trial data, and reporting of clinical research data for studies focused on women's health, aging, and marginalized populations.
Role type
Senior Clinical Research Coordinator / Research Project Manager
Builds
Clinical trials, research studies, manuscripts, and reports
Domain
Health services research, women's health, aging, public health
Required skills
Clinical trial management, IRB protocol development, regulatory compliance (FDA, NIH, HIPAA), quantitative and qualitative data analysis, grant writing, participant recruitment, literature search and synthesis, data management, project management, training and supervision of research staff
Preferred skills
Master's degree in health services research or related field, expertise in women's sexual health and social determinants of health, proficiency in STATA, R, or equivalent programs, experience with qualitative data analysis using ATLAS-TI, expertise in investigator-initiated clinical trials, NIH grant writing
Technologies
STATA, R, ATLAS-TI, clinicaltrials.gov, Florence portal
Responsibilities
Design, develop, and implement quantitative and qualitative research studies; manage high complexity clinical studies including scientific planning and execution; perform data collection, preparation, management, and analysis; prepare and lead presentations and manuscripts; conduct and supervise literature searches; track data collection progress and identify deviations; support regulatory and administrative activities including IRB protocols; train and supervise research trainees; manage daily administrative and technical activities in complex clinical trials; implement Good Clinical Practices (GCP) and relevant laws; solve complex problems relating to data management and analysis of large administrative datasets; act as a resource on clinical research basics for colleagues
Seniority
Senior, hands-on IC