-5 - 8 years relevant experience working as a clinical research coordinator role (project manager, research assistant, study coordinator, etc.) and/or working as an IRB analyst/human subjects protection, or Master's and 3 or more years of relevant experience. - Experience with conduct of clinical research with pharmaceutical/device clinical trials and/or observational or socio behavioral and/or public health research. - Experience/knowledge of IRB applications and managing IRB submission efforts. - Prior experience working as IRB staff is beneficial to the job, but not required. - Excellent interpersonal and communication skills required. - Detail oriented. Ability to multi-task and facilitate collaborations across various BU/BMC administrative and research departments. - Strong computer skills, including experience with databases, spreadsheets, Microsoft PowerPoint, word processing, etc.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. We are a VEVRAA Federal Contractor.