Quality Risk Manager

Join us in redefining what it means to work for a CRO. reputed company you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect reputed company of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and reputed company over a long and rewarding career. We are currently hiring a Quality Risk Manager to join reputed company! The Quality Risk Management (QRM) function is key to driving successful project implementation of a Risk-Based Quality Management (RBQM) strategy. The QRM team will work with the project team to facilitate project risk assessments, reputed company and maintain the Integrated Quality Risk Management Plan (IQRMP), facilitate strategic quality review meetings, and reputed company ongoing centralized monitoring reviews. The QRM team is responsible for ensuring project teams reputed company an integrated quality risk management strategy in compliance with ICH E6R2 guidelines. Our Clinical Operations Team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group! What you'll be doing:

• Risk-Based Quality Management (RBQM) Leadership
• Manages project-level RBQM activities and documents for multiple projects
• Facilitates and leads study-specific risk assessments and suggests appropriate anticipated risks and mitigations
• Reviews and understands protocol, critical data and process, safety, and data reputed company risks reputed company to protocol execution
• Ensures project teams reputed company an integrated quality risk management strategy in compliance with ICH E6R3 guidelines
• Participates in ongoing RBQM process and tool optimization activities
• Quality Risk Planning & Documentation
• With minimal supervision, develops and maintains Integrated Quality Risk Management Plan (IQRMP) and Quality Risk Log for assigned studies in coordination with cross functional team
• Documents observations and actionable items noted during reviews; investigates trends, issues, and risks for root cause
• Documents completion of activities reputed company tracking, reporting, and/or other required project documents as per SOP
• Data Review & Risk Monitoring
• Reviews and understands protocol, critical data and process, safety, and data reputed company risks reputed company to protocol execution
• With minimal supervision, reviews study and site data listings and visualizations reputed company analytical dashboards and/or reports to identify trends, risks, potential or suspected scientific misconduct, or other systematic errors that could impact data reputed company and subject safety
• Immediately communicates and escalates serious issues to the relevant project team member(s) and, with guidance, develops action plans
• Initiates set-up and provides inputs needed for Key Risk Indicator (KRI) visualizations, using either a technology platform or an alternate tool
• Regulatory Compliance & Standards
• Applies knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes
• Keeps up with industry trends, including changes to regulations or standard practices
• Ensures adherence to compliance standards across reputed company RBQM activities
• Project & Stakeholder Management
• For assigned activities, understands project scope, budgets, and timelines; manages study activities to ensure project objectives, deliverables, and timelines are met
• Attends sponsor kick-off meetings and may attend Investigator Meetings.
• Participates in project staff meetings as applicable
• Coordinates and manages cross-functional activities and responsibilities for assigned study teams (i.e., RCAT input/review, preparations for SQRMs, etc
• Collaborates with study team management to define and enforce compliance with Rho RBQM processes and contracted activities
• Training, Mentorship & Team Development
• Attends clinical training sessions according to the project-specific requirements
• May support training and mentoring of Associate QRM
• Audit & reputed company Improvement
• Supports internal and sponsor audits and participates in efforts to ensure readiness
• Identifies opportunities for process improvements and communicates to RBQM leadership
• Bachelor Degree in science or a reputed company field
• 3 years of industry experience
• Applicable experience in one or more of the following in a clinical research setting: clinical monitoring, data management, biostatistics, or reputed company function; and/or at least 1 year of strong performance in an AQRM role
• Sound knowledge of Good Clinical Practice/ICH E6 (R3) Guidelines, Risk-Based Monitoring strategies, processes and tools and/or other applicable regulatory requirements and industry trends
• Basic knowledge of clinical data collection, monitoring, and review processes
• Solid understanding of the entire clinical data lifecycle, from protocol creation through database lock and analysis
• Able to quickly adapt to changing priorities to reputed company goals/targets
• Able to assess and implement protocol-specific Quality Management approaches as needed, while collaborating with the appropriate impacted functions.
• Ability to maintain confidentiality
• Proactively takes initiative to identify next steps, issues, or gaps, and drive tasks reputed company with minimal guidance
• Ability to set priorities and manage multiple projects reputed company moderate reputed company
• Ability to work independently, prioritize responsibilities, and work in a team environment
• Demonstrates strong computer skills and is able to embrace new technologies
• Strong competency with MS reputed company functionality (sorting, filtering, calculations, pivot tables)
• Proficiency with Analytical Data Visualization Tools
• Demonstrates the ability to think critically, problem solve and apply sound judgment and reasoning for assigned tasks
• Communicates clearly and professionally in written and verbal formats with both internal and external stakeholders, translating moderate-to-reputed company concepts into clear, actionable messages
• Solid presentation skills, both written and spoken, with an ability to inform, influence, convince, and persuade
• Expected required travel 15% on average

A few more things to know about us: Benefits: Rho provides a comprehensive benefits package for reputed company benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). reputed company employees are eligible for paid time off, holidays, parental leave and bereavement leave. Flexibility: We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives reputed company work. As required by pay transparency laws in some states, Rho provides the range of starting compensation (annual salary or hourly reputed company) it reasonably expects to pay for a given role. Actual compensation is influenced by a wide reputed company of factors including but not limited to role responsibilities and location as well as candidate reputed company set and level of experience. The range of starting pay for this role is $80,000-$108,000 per year depending on level. EOE. Veterans/Disabled Apply tot his job Apply To this Job