November 13
β’ Technical writing, compliance discovery/adherence, and audit initiation/tracking/support β’ Required to stay abreast of current industry standards β’ Self-motivated with autonomous work expectations β’ Support the scope and values of BRSI β’ Report directly to the Software Quality Assurance Coordinator/Compliance Officer β’ Develop/Revise comprehensive user-friendly content that meets the needs of target audiences β’ Translate complex information into simple, polished, engaging content
β’ Understanding of regulatory frameworks/reporting β’ Strong research skills with superior content retention with proven capability to quickly learn and understand complex subject matters β’ Related experience as an effective technical writer and compliance analyst β’ Experience in writing documentation and procedure manuals/policies/plans for various audiences β’ Superb written and communication skills, with a keen eye for detail β’ Experience with product development β’ Ability to prioritize multiple simultaneous deadlines β’ Experience with industry standards including (but not limited to) NIST 800-53, 800-171, CMMC, CMS, SOC, SSAE18, RMF, HIPAA, ADA (section 508), FedRAMP/StateRAMP, FISMA, and CUI β’ Direct experience with healthcare-related services and standards as pertaining to various levels of federal, state, local, commercial, and private contracting β’ Firm understanding of SDLC (systems development lifecycle) and previous experience in software development β’ Experience with Inflectra project management/reporting software and LeapWork testing software
β’ 40 Hour work week expected (no overtime authorized) β’ Mainly conducted Monday β Friday β’ Very occasional weekend work β planned and coordinated well in advance of duty performance (no last minute/on call/emergency requirements) β’ Semi-flexible duration of daily work hours β’ Remote work possible AFTER probationary period β’ Paid vacation β’ Medical/Dental/Vision/401K
Apply NowNovember 9
Join Chartis as a healthcare consultant in compliance consulting.
πΊπΈ United States β Remote
π΅ $185k - $225k / year
π° Private Equity Round on 2012-12
β° Full Time
π’ Junior
π‘ Mid-level
π Compliance
November 9
Regulatory Analyst II overseeing clinical trial regulatory submissions at University of Miami.
πΊπΈ United States β Remote
π° $1M Grant on 2023-02
β° Full Time
π’ Junior
π‘ Mid-level
π Compliance
π¦ H1B Visa Sponsor
November 7
Manage Utilization Review licensing and compliance at Premier, a healthcare improvement company.
πΊπΈ United States β Remote
π΅ $51k - $95k / year
β° Full Time
π’ Junior
π‘ Mid-level
π Compliance
π«π¨βπ No degree required
October 17
Drive FDA regulatory strategy business for Avalere Health through client relationships.
September 18
Compliance role reviewing accounts at Gemini's crypto and Web3 platform.
πΊπΈ United States β Remote
π΅ $75k - $93k / year
β° Full Time
π’ Junior
π‘ Mid-level
π Compliance
π¦ H1B Visa Sponsor