Sr. Director, Clinical Data Management

ALX Oncology Inc.•South San Francisco, CA

4d•$240,000 - $280,000•Hybrid

About The Position

Reporting to the VP, Biometrics, the Sr. Director, Clinical Data Management provides strategic and operational leadership for the Clinical Data Management function across ALX Oncology's development portfolio. As the senior data management leader in a lean biotechnology environment, this individual is responsible for establishing a scalable, fit-for-purpose function that delivers high-quality clinical trial data to support development milestones, regulatory submissions, and future portfolio growth. This role requires a leader who can think strategically while remaining hands-on, building effective partnerships and driving operational excellence in a dynamic, resource-focused organization. Preference will be given to candidates who can regularly work onsite Mondays and Tuesdays as part of the company's hybrid work model.

Requirements

Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related scientific discipline, or an equivalent combination of education and directly relevant work experience.
Approximately 12+ years of progressive Clinical Data Management experience within biotechnology, pharmaceutical, or CRO environments, including Phase I-III clinical studies, with demonstrated success leading outsourced Clinical Data Management activities, partnering across functions, and delivering high-quality clinical trial data.
Experience supporting regulatory submissions is preferred.
Oncology and/or immuno-oncology experience is strongly preferred.
Strong knowledge of Clinical Data Management principles, GCP, applicable regulatory requirements, CDISC standards, and industry best practices, with demonstrated expertise in database design, data cleaning, medical coding, external data reconciliation, data review, database lock, and other core Clinical Data Management processes.
Experience with leading EDC platforms such as Medidata Rave, Veeva EDC, Oracle Clinical, or equivalent systems.
Demonstrated ability to effectively manage CROs, vendors, budgets, and outsourced Clinical Data Management activities.
Strategic, collaborative leader with excellent communication, organizational, and relationship-building skills, capable of influencing cross-functional teams and external partners.
Demonstrated ability to prioritize competing demands, solve complex problems, build scalable processes, and adapt to evolving business priorities while contributing beyond functional boundaries in a fast-paced, resource-constrained environment.

Nice To Haves

Advanced degree (MS, MPH, PhD) is a plus.

Responsibilities

Lead the Clinical Data Management function by developing and executing strategies, processes, and operational plans that support ALX Oncology's clinical development portfolio and align with the objectives of the Biometrics organization.
Oversee Clinical Data Management activities across the development portfolio, including review and approval of key deliverables such as database design, eCRFs, edit checks, data review plans, and database lock activities.
Lead data review, issue management, and milestone readiness to support interim analyses, database locks, and key development milestones.
Serve as the primary escalation point for data management issues affecting study quality, timelines, or regulatory readiness.
Oversee EDC and related clinical data systems, including implementation, configuration, and vendor management.
Lead the selection, oversight, and performance management of CROs and specialty vendors, establishing governance, performance metrics, and communication processes to ensure high-quality execution and accountability.
Manage vendor budgets and identify cost-effective solutions without compromising quality or compliance.
Drive continuous improvement initiatives that enhance data quality, operational efficiency, and study execution.
Partner with Clinical Operations, Biostatistics, Statistical Programming, Clinical Science, Medical, Safety, Regulatory, and Quality to support successful study execution.
Provide data management expertise during protocol development, advising on data collection strategy, endpoint feasibility, and study design.
Ensure clinical data are inspection-ready and support regulatory submissions, audits, safety reviews, and due diligence activities.
Contribute to a culture that reflects ALX's values by acting with integrity, accountability, transparency, and respect. Build strong, collaborative relationships through active engagement with colleagues, including regular onsite participation consistent with the company's hybrid work model.