Director, Clinical Quality Assurance Solid BiosciencesSolid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care.Patient-focused and founded by those directly impacted by Duchenne, Solid's mission is to improve the daily lives of patients living with devastating rare diseases.We are seeking a Clinical Quality Assurance (CQA) Director who is responsible for establishing, implementing, and maintaining quality systems and risk?management practices that ensure clinical trials are conducted in compliance with ICH?GCP, applicable regulatory requirements, internal SOPs, and industry best practices.The individual is this role is responsible for quality management and oversight of clinical trials, clinical audit program, and risks across the clinical portfolio, in partnership with cross?functional teams to proactively improve quality and trial execution.This role will report to the Head of Quality. The position is remote and full time. Solid's Corporate Headquarters is located in Hood Park in Charlestown, MA and it is preferred that the individual in this role be available to come on-site periodically throughout the year.Key Position ResponsibilitiesQuality Oversight & ComplianceDevelop, implement, and maintain the Clinical Quality Management System (CQMS) to support inspection readiness and regulatory compliance.Provide GCP compliance oversight to all clinical programs, including CROs, clinical sites, vendors, and internal teams.Review clinical documentation (protocols, monitoring plans, TMF, vendor deliverables, etc.) to ensure compliance and quality.Serve as a subject matter expert (SME) for GCP and clinical quality best practices.Audit & Inspection ReadinessPlan, execute, and report on internal and external audits (e.g., sites, vendors, TMF, system audits).Track and support resolution of audit findings and CAPAs.Lead preparation for regulatory inspections (FDA, EMA, MHRA, etc.).Facilitate mock inspections, training, and inspection logistics.Risk ManagementLead clinical risk assessments using quality-by-design (QbD) and risk-based quality management (RBQM) principles.Identify systemic risks across the clinical trial portfolio and implement risk mitigation strategies.Monitor key quality indicators (KQIs), KPIs, deviations, and other signals to detect emerging risks.Partner with Clinical Operations and Data Management to evaluate and escalate risks proactively.Vendor & Site OversightEvaluate and qualify CROs and key service providers from a quality perspective.Perform vendor audits when needed and oversee vendor risk assessments.Partner with Clinical Operations to ensure oversight plans are robust and followed.Training & Continuous ImprovementConduct GCP and quality training for clinical staff, CROs, and investigators.Develop and maintain SOPs, work instructions, guidance documents, and quality tools.Lead quality improvement initiatives and support continuous process optimization.Foster a culture of quality, compliance, and proactive risk management throughout the organization.Documentation & ReportingPrepare clear, concise reports summarizing audit outcomes, risk assessments, and quality metrics.Ensure timely and accurate documentation in the Trial Master File (TMF).Present quality trends, risks, and recommendations to management and cross?functional teams.Experience RequirementsBachelor's degree in life sciences, nursing, pharmacy, or related field.510+ years of experience in clinical research, with a minimum of 3 years in Quality Assurance or Clinical Compliance.Deep knowledge of ICH?GCP, FDA, EMA, and other global clinical regulatory requirements.Experience conducting clinical site, vendor, and/or system audits.Strong understanding of risk?based monitoring and QbD principles.Excellent communication, problem?solving, and relationship?building skills.Key Position AttributesAnalytical and strategic thinking to identify and address quality risks.Attention to detail and strong documentation habits.Diplomacy and collaboration, working effectively across functions.Proactive problem?solving with a continuous improvement mindset.Ability to manage multiple priorities in a fast?paced environment.CompensationThe base compensation range for this role is: $197,000 - $233,700Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid's long term company performance.Benefits and Solid AdvantagesCompetitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs401(k) program participation with competitive company matched contributionsEligibility to participate in Solid's Employee Stock Purchase PlanMobile phone subsidy for eligible employeesTuition ReimbursementVision CoverageLife InsuranceVoluntary Pet InsuranceEmployee Discount Program on Travel, Entertainment, and ServicesDaily Subsidized Lunch Delivery (onsite @ Hood Park)Free Onsite Full-Service Gym (onsite @ Hood Park)Employee Parking (onsite @ Hood Park)