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FormativGroup

Business Analyst – Regulatory Affairs / RIM at FormativGroup

Hybrid/Richmond, VA - Full - TimeFull-time5120-Staff AugmentationPosted 10 days ago
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About the Role

<h3>Is this you?</h3> <p>Are you a Regulatory Affairs Business Analyst who can translate complex regulatory and business needs into clear requirements, process flows, and system-ready documentation? This role is ideal for someone with deep Regulatory Affairs experience who enjoys partnering across business and technology teams to help drive a successful Regulatory Information Management (RIM) implementation.</p> <h3>About the role</h3> <p>The Business Analyst - Regulatory Affairs / RIM will support the business side of a Regulatory Information Management system implementation, serving as a bridge between Regulatory Affairs stakeholders and the teams responsible for delivering the solution.</p> <p>In this role, you’ll gather and document business requirements, develop current- and future-state process flows, facilitate stakeholder discussions, and translate regulatory processes into clear, actionable requirements for the RIM implementation.</p> <p>This is <strong>not a regulatory submissions production role</strong>. Rather than compiling or submitting documents directly to the FDA or other Health Authorities, you’ll use your Regulatory Affairs expertise to help business and technology teams understand regulatory workflows, requirements, and documentation needs so the RIM solution effectively supports the business.</p> <p>&nbsp;</p> <p><span style="font-size: 12pt;"><strong>What You'll Work On<br><em>As Business Analyst – Regulatory Affairs / RIM, you will:</em></strong></span></p> <ul> <li><span style="font-size: 12pt;">Lead or support the business in gathering, organizing, and documenting requirements for a RIM system deployment.</span></li> <li><span style="font-size: 12pt;">Create, update, and maintain process flows that reflect Regulatory Affairs business processes and system needs.</span></li> <li><span style="font-size: 12pt;">Collaborate with Regulatory Affairs stakeholders, business users, technology teams, and implementation partners to clarify requirements and priorities.</span></li> <li><span style="font-size: 12pt;">Support stakeholder discussions, workshops, and working sessions to understand current-state and future-state processes.</span></li> <li><span style="font-size: 12pt;">Translate regulatory business needs into clear business requirements, process documentation, and system-supporting materials.</span></li> <li><span style="font-size: 12pt;">Apply Regulatory Affairs subject matter expertise to help teams understand Health Authority regulations, regulatory workflows, and RIM-related needs.</span></li> <li><span style="font-size: 12pt;">Support documentation related to regulatory submissions processes, annual reports, Health Authority conversations, and related regulatory activities as they connect to the RIM system.</span></li> <li><span style="font-size: 12pt;">Help compile and organize documents needed to support a RIM system implementation, including business requirements and related process materials.</span></li> <li><span style="font-size: 12pt;">Use tools such as Word, Excel, PowerPoint, and Visio to document requirements, process flows, stakeholder inputs, and project materials.</span></li> <li><span style="font-size: 12pt;">Partner with cross-functional teams to ensure business requirements are understood, traceable, and aligned to implementation goals.</span></li> </ul> <p>&nbsp;</p> <p><span style="font-size: 12pt;"><strong>What You'll Bring<br><em>You will likely be successful in this role if you have:</em></strong></span></p> <ul> <li><span style="font-size: 12pt;">10+ years of Regulatory Affairs experience, with direct experience working in regulatory affairs required.</span></li> <li><span style="font-size: 12pt;">Regulatory Information Management experience required.</span></li> <li><span style="font-size: 12pt;">Experience supporting or working with RIM systems, RIM processes, or RIM system deployments.</span></li> <li><span style="font-size: 12pt;">Experience with Health Authority regulations, ideally FDA regulations applicable to the tobacco industry.</span></li> <li><span style="font-size: 12pt;">Experience with Health Authority regulations in pharma or medical device environments, with willingness to learn tobacco regulations, may also be considered.</span></li> <li><span style="font-size: 12pt;">Experience with regulatory submissions processes, including annual reports and Health Authority communications or conversations.</span></li> <li><span style="font-size: 12pt;">Strong stakeholder management experience, including the ability to work with business users, regulatory teams, technical teams, and project stakeholders.</span></li> <li><span style="font-size: 12pt;">Experience gathering requirements, documenting business needs, and supporting process documentation for system implementation work.</span></li> <li><span style="font-size: 12pt;">Know-how of compiling documents for a RIM system, including business requirements and related implementation materials.</span></li> <li><span style="font-size: 12pt;">Proficiency with Microsoft Word, Excel, PowerPoint, and Visio.</span></li> </ul> <p>&nbsp;</p> <p><span style="font-size: 12pt;"><strong>How You Work</strong></span></p> <ul> <li><span style="font-size: 12pt;">You are business-focused, practical, and able to translate regulatory knowledge into clear requirements and process documentation.</span></li> <li><span style="font-size: 12pt;">You are comfortable working with multiple stakeholders, asking thoughtful questions, and clarifying details in a structured way.</span></li> <li><span style="font-size: 12pt;">You bring strong attention to detail, clear communication, and a collaborative mindset to implementation work that requires accuracy, alignment, and follow-through.</span></li> </ul> <p>&nbsp;</p> <p><span style="font-size: 12pt;"><strong>Bonus Points If You Have</strong></span></p> <ul> <li><span style="font-size: 12pt;">Experience with tobacco regulatory requirements or FDA regulations applicable to tobacco products.</span></li> <li><span style="font-size: 12pt;">Experience supporting RIM system implementation, deployment, migration, or optimization projects.</span></li> <li><span style="font-size: 12pt;">Experience documenting current-state and future-state regulatory processes.</span></li> <li><span style="font-size: 12pt;">Experience working in pharma, medical device, tobacco, or other highly regulated product environments.</span></li> <li><span style="font-size: 12pt;">Experience using business process modeling tools beyond Visio.</span></li> </ul> <p>&nbsp;</p> <p><strong><span style="font-size: 12pt;">What Success Looks Like</span></strong></p> <ul> <li><span style="font-size: 12pt;">Regulatory Affairs requirements are clearly gathered, documented, and aligned to the RIM system deployment.</span></li> <li><span style="font-size: 12pt;">Process flows and business documentation accurately reflect stakeholder needs and regulatory workflows.</span></li> <li><span style="font-size: 12pt;">Business, regulatory, and technology teams have a shared understanding of requirements, priorities, and implementation expectations.</span></li> <li><span style="font-size: 12pt;">Stakeholders view you as a trusted Regulatory Affairs SME who can bridge business needs and system implementation work.</span></li> <li><span style="font-size: 12pt;">Your work helps support a smoother, more organized, and business-aligned RIM deployment.</span></li> </ul> <p>&nbsp;</p> <p><span style="font-size: 12pt;"><strong>Why Join FormativGroup<br></strong>FormativGroup is a PE-backed technology consulting and implementation partner helping organizations modernize complex business platforms, improve delivery outcomes, and scale technology solutions that support long-term growth. We partner with clients across strategy, solution design, implementation, and ongoing support to help move critical initiatives from vision to execution. Our teams bring deep technical expertise, delivery discipline, and a collaborative approach to every engagement.</span></p> <p><span style="font-size: 12pt;">At FormativGroup, you'll work with people who are practical, collaborative, and focused on solving meaningful business and technology problems. We're growing, which means you'll have opportunities to contribute ideas, work closely with experienced leaders, and help shape how we deliver for clients.</span></p> <p>&nbsp;</p> <p><span style="font-size: 12pt;"><strong>Employment Eligibility<br></strong></span></p> <ul> <li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">This role is Hybrid, must reside near to Richmond, VA - Not open to travel - must go onsite 1st week and intermittently</span></p> </li> <li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> <p><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa now or in the future.</span></p> </li> <li style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">To be considered for this position, candidates must reside in one of the following U.S. states: MA, NC, VA, and Washington DC. Candidates residing outside these states are not eligible for consideration currently</span></li> </ul> <p>&nbsp;</p> <p>&nbsp;</p><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p><span data-contrast="auto">We are committed to pay equity and transparency. The compensation range for this position represents our good faith estimate of the range we reasonably expect to pay for this role at the time of posting. The actual compensation offered will be determined based on factors such as the candidate’s experience, skills, education, work location, and internal equity.</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559685&quot;:720,&quot;335559739&quot;:200,&quot;335559740&quot;:276}">&nbsp;</span></p> <p><span data-contrast="auto">In addition to hourly pay, employees may be eligible for discretionary bonuses, commissions, or other incentive programs, as well as a comprehensive benefits package that includes medical, dental, vision, 401(k), paid time off, etc.</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559685&quot;:720,&quot;335559739&quot;:200,&quot;335559740&quot;:276}">&nbsp;</span></p></div><div class="title">Estimated hourly Compensation Range:</div><div class="pay-range"><span>$85</span><span class="divider">&mdash;</span><span>$95 USD</span></div></div></div><div class="content-conclusion"><p><span data-contrast="none">FormativGroup&nbsp;operates within the critical middle layer of business technology, where applications and systems connect infrastructure to business processes. We are specialists who help the middle market take full advantage of their technology investments with deep, industry-centric&nbsp;expertise, all in one place, to unify fragmented systems.&nbsp;</span><em><span data-contrast="none">With deep technical&nbsp;expertise&nbsp;across cloud architecture, system integration, AI, and data strategy, we bridge the gap between business goals and modern platforms.</span></em><span data-contrast="auto">&nbsp;</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559685&quot;:720,&quot;335559739&quot;:200,&quot;335559740&quot;:276}">&nbsp;</span></p> <p><span data-contrast="auto">FormativGroup is an equal opportunity employer providing opportunities to applicants and employees without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.</span></p> <p><span data-contrast="auto">ADA Specifications: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559685&quot;:720,&quot;335559739&quot;:200,&quot;335559740&quot;:276}">&nbsp;</span></p> <p><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559685&quot;:720,&quot;335559739&quot;:200,&quot;335559740&quot;:276}"><span class="TextRun SCXW90414986 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW90414986 BCX0">#formativgroupcareers #WorkWithUs</span></span></span></p> <p>&nbsp;</p> <p><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335559685&quot;:720,&quot;335559739&quot;:200,&quot;335559740&quot;:276}"><span class="TextRun SCXW90414986 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW90414986 BCX0">Click here to view our <a href="https://formativgroup.io/2025/11/19/privacy-policy/" target="_blank">Privacy Policy</a></span></span></span></p></div>