Associate Director, GCP Quality Assurance

<div class="content-intro"><p><span style="text-decoration: underline;"><strong>About Beeline Medicines:</strong></span></p> <p>Beeline Medicines is a clinical‑stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients – realizing a world where people with immune-mediated diseases can live life fully.</p></div><p><span style="text-decoration: underline;"><strong>Job Summary:</strong></span></p> <p>The Associate Director, GCP Quality Assurance is responsible for providing strategic and operational Quality Assurance oversight for Good Clinical Practice (GCP) activities supporting the company’s clinical development programs. This role ensures that clinical trials are conducted in compliance with applicable regulatory requirements, company policies, and global GCP standards, with a continuous state of inspection readiness.</p> <p>The Director partners closely with Clinical Operations, Regulatory Affairs, Pharmacovigilance, Data Management, and external service providers to implement a risk-based quality oversight model across the clinical lifecycle. The role is accountable for GCP quality systems, vendor oversight, audits, and inspection support, and plays a critical role in embedding quality by design into clinical development programs.</p> <p><span style="text-decoration: underline;"><strong><br>Work Arrangement &amp; Location:&nbsp;</strong></span></p> <p><strong>Hybrid</strong> - This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week — currently designated as&nbsp;<strong>Tuesday and Wednesday</strong>. Additional on-site days may be required based on business needs, team priorities, or leadership direction.</p> <p><span style="text-decoration: underline;"><strong><br>Essential Duties and Responsibilities: </strong></span></p> <ul> <li>Develop and implement the GCP QA strategy aligned with clinical development objectives and global regulatory expectations</li> <li>Serve as a key QA partner to Clinical Operations and cross-functional stakeholders on GCP compliance and quality risk management.</li> <li>Promote a strong culture of quality, compliance, and continuous improvement across clinical programs.</li> <li>Oversee GCP quality systems including deviations, investigations, CAPAs, change control, documentation, and training related to clinical activities.</li> <li>Ensure GCP processes are phase-appropriate, compliant, and scalable.</li> <li>Support the development, review, and approval of GCP-related SOPs, policies, and work instructions.</li> <li>Provide QA oversight for GCP activities conducted internally and by CROs, vendors, and other service providers.</li> <li>Lead GCP vendor qualification, audit strategy, and ongoing oversight using risk-based principles.</li> <li>Review and approve GCP-related quality agreements and vendor oversight plans.</li> <li>Plan and execute risk-based GCP audits, including CRO audits, investigator site audits, and system audits as applicable</li> <li>Lead GCP inspection readiness activities and serve as a primary QA contact during health authority inspections.</li> <li>Coordinate inspection preparation, conduct, and follow-up, including responses to regulatory observations.</li> <li>Perform other duties and responsibilities as assigned.</li> </ul> <p><span style="text-decoration: underline;"><strong><br>Qualifications:</strong></span></p> <ul> <li>Education: Bachelor's degree required in a scientific or technical discipline (Life Sciences, Chemistry, Engineering, or related field); advanced degree strongly preferred.</li> <li>7+ years of experience in GCP Quality Assurance or Clinical Quality within a biotech or pharmaceutical environment.</li> <li>Strong knowledge of global GCP regulations and clinical trial oversight requirements.</li> <li>Demonstrated experience supporting regulatory inspections and audits.</li> <li>Experience overseeing CROs and other GCP service providers.</li> <li>Experience supporting late-stage or pivotal clinical trials.</li> <li>Strong background in risk-based quality management and inspection readiness.</li> <li>Ability to balance compliance with operational execution</li> <li>Commitment to patient safety, data integrity, and quality culture</li> <li>Strong cross-functional collaborator who proactively communicates quality risk, escalates issues with appropriate context and urgency, and fosters a culture of transparent, solution-oriented dialogue.</li> </ul><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p class="p1"><span style="text-decoration: underline;"><strong>Salary Range:</strong></span></p> <p class="p1"><span data-teams="true">The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.</span></p></div><div class="title">Salary Range</div><div class="pay-range"><span>$165,750</span><span class="divider">&mdash;</span><span>$214,500 USD</span></div></div></div><div class="content-conclusion"><p><span style="text-decoration: underline;"><strong>Benefits:</strong></span></p> <p></p> <p>We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:</p> <ul> <li>Competitive health and wellness coverage (structure and premiums vary by country)</li> <li>Paid time off, public holidays, and additional leave entitlements in accordance with local requirements</li> <li>Flexible work arrangements / hybrid schedule</li> </ul> <p><em>Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.</em></p> <p><span style="text-decoration: underline;"><strong>Equal Employment Opportunity:</strong></span></p> <p><em>Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.</em></p> <p><span style="text-decoration: underline;"><strong>Reasonable Accommodation:</strong></span></p> <p>If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.</p> <p><strong><span style="text-decoration: underline;">Privacy</span><br><br></strong>Upon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at <a href="https://beelinemedicines.com/privacy-policy/">Privacy Policy - Beeline Medicines</a></p></div>