Position Summary The Division of Adolescent/Young Adult Medicine is seeking a Clinical Research Coordinator to work with faculty researcher Sabra L. Katz-Wise, PhD and the GenderWise Lab. We are looking for someone who is passionate about LGBTQ+ adolescent/young adult health and has interest and experience in both qualitative and survey research. This position will provide support across several different research projects, including a study about stigma and health of bisexual adolescents/young adults and a study expanding an online intervention for families with transgender and nonbinary adolescents.
A written expression of interest included with your application is highly appreciated.
Key Responsibilities:
Project management for GenderWise Lab studies (e.g., tracking and reporting progress and expenses, managing IRB protocols, maintaining staff procedure guides)
Serving as the liaison between the GenderWise Lab and external organizations for contracts, data use agreements, and other activities to advance research aims
Recruitment and screening of study participants
Maintaining study data in accordance with data management and sharing protocols
Coding and analyzing qualitative data and contributing to quantitative data analysis, as skills allow
Conducting literature reviews and contributing to writing research manuscripts and reports
Helping to prepare grant applications for submission. Ongoing facilitation of a community advisory board
Maintaining the GenderWise Lab website. Coordinating and scheduling meetings, submitting receipts for reimbursement, completing CV-related tracking forms
Onboarding and training staff and students on GenderWise Lab and BCH procedures
Minimum Qualifications Education:
A bachelor's degree in a related field; a master's degree preferred
Experience:
2 years of experience as a Research Assistant, Research Coordinator, or Lab Manager
Detail-oriented with strong project management and organizational skills
Ability to take initiative, work without direct supervision, work on multiple projects simultaneously, and meet deadlines
Ability to maintain participant data confidentiality and adhere to study protocols
Strong verbal and written communication skills
Ability to collaborate and work well with others
Experience and comfort using standard computer software (e.g., Microsoft Office and Google programs)
Preferred Experience:
Prior advocacy for and/or allyship with LGBTQ+ communities, particularly bisexual communities and transgender and nonbinary communities
Prior experience with qualitative research
Prior experience with IRB protocols
Experience and comfort using survey building tools (e.g., REDCap), analysis software (e.g., SPSS, Dedoose), and website management tools (e.g., Google Sites, Wordpress)