Director, Clinical Operations

amylyx; Cambridge (MA); On-site; USD 140,000 - 210,000; Full time

Job summary

Amylyx is seeking a Director of Clinical Operations to lead end-to-end execution of global clinical studies in a fast-paced, small-company environment.

The role requires senior-level ops leadership, experience managing CROs and vendors, and a strong focus on timelines, budget, quality, and patient safety. Collaboration with Regulatory, Data Management, and Finance is essential.

Qualifications

• 12+ years of clinical operations experience in pharmaceutical/biotech.
• Experience with ICH-GCP guidelines and GDPR compliance.
• Experience leading study teams and overseeing external partners.

Responsibilities

• Provide end-to-end operational leadership for global clinical trials across full study lifecycle.
• Oversee development of integrated study operational plans with timelines and resources.
• Identify risks and ensure mitigation, escalation, and timely resolution.
• Ensure data integrity, quality, and compliance with SOPs and regulations.
• Manage CROs, vendors, and outsourcing strategies with cross-functional stakeholders.
• Mentor and develop clinical operations team members.

Skills

Clinical operations leadership

Global trials

CRO management

Risk management

Budget oversight

Study documentation

Education

BS/BA in science or health-related field

Job description

Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).

Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply.

The Opportunity

The Director, Clinical Operations is a senior member of the Amylyx Global Clinical Operations team responsible for the operational strategy, planning, execution, and oversight of assigned global clinical studies. Therapeutic areas may include: Post Bariatric Hypoglycemia or other associated conditions, Amytrophic Lateral Sclerosis (ALS), Wolfram Syndrome and/or other diseases under study at Amylyx Pharmaceuticals.

This individual will provide end to end operational leadership for clinical trials, working with a high degree of independence in a small, fast-paced company environment. The Director will translate program and study strategy into executable operational plans and ensure delivery against timelines, budget, quality and compliance expectations.

The ideal candidate is an experienced clinical operations leader with demonstrated success managing complex global clinical trials, CROs, functional service providers and specialty vendors. This individual is proactive, solutions oriented, comfortable making risk-based decisions, and able to identify emerging issues before they impact study execution.

The Director will work closely with Clinical Operations leadership, Clinical Development, Regulatory, Data Management, Biostatistics, Pharmacovigilance, Clinical Compliance, Quality, Clinical Outsourcing, Finance, Legal and other internal functions while providing strong oversight and direction to external partners.

This individual should be a proactive problem-solver with proficient verbal and written communication skills, comfortable leading study teams working with ambitious timelines. The ideal candidate will also have previous experience managing clinical operations team members, and helping to shape their growth and development.

Responsibilities

• Provide end-to-end operational leadership and accountability for assigned global clinical trials for the full study lifecycle with close attention to effective planning and execution, risk management, data integrity, quality and compliance with Company SOPs, ICH-GCP guidelines, GDPR, and other regulations and patient safety standards.
• Oversee development and maintenance of integrated study operational plans, including timelines, enrollment assumptions, resource requirements, key dependencies, risks and contingency plans.
• Drive execution against study milestones, proactively identifying risks, issues, trends, and interdependencies and ensuring appropriate mitigation, escalation and resolution.
• Ensures appropriate operational procedures are implemented or adhered to, to assure high quality trial data and operational excellence of assigned studies.
• Develops, analyses, and reports on metrics for clinical programs.
• In conjunction with Clinical Leadership, ensures study deliverables are achieved on time and within budget.
• Contributes to the development of study documentation including protocols, study manuals, ICFs, CRFs, Clinical Study Reports etc.
• Communicates trial status, issues, mitigations, and lessons learned to relevant cross-functional stakeholders, including senior leadership.
• Stakeholder in CRO and vendor selection. Works with clinical operations leadership, clinical outsourcing, legal, and finance in the development of effective outsourcing strategies, including selection and contracting of CROs and vendors. Oversees and contributes to financial reporting for assigned projects including but not limited to PO management, projections, actuals and accruals.
• Manages relationships and establishes strong partnerships with CROs, vendors, investigators, and other external partners.
• Addresses and/or escalates vendor performance issues; identifies probable vendor risks and potential mitigation strategies.
• Develops SOPs, work instructions, and standardized forms to define Clinical Operations processes within a growing team.
• Provides leadership and support to direct report(s), if applicable, including mentoring, training, performance evaluation, and career development.

Requirements

• BS/BA Degree, in science or a health-related field is preferred.
• Minimum of 12 years of clinical operations experience in a pharmaceutical/biotec