Jobs at Apogee Therapeutics

Manage logistics of biomarker sample collection, ensure adherence to clinical protocols, oversee data transfer, vendor management, and budget tracking for clinical trials.

The Senior Manager of Clinical Systems oversees clinical technology initiatives, manages clinical systems projects, ensures compliance, and promotes process adoption across multiple functions while collaborating with various stakeholders.

The Director of Clinical Development will oversee clinical trials in inflammation and immunology, collaborating with cross-functional teams, ensuring protocol adherence, and providing scientific insights for decision-making.

The Director of US Insights and Market Development will lead market research initiatives, develop strategies for pre-launch and brand activities, and integrate insights from various analytics to support decision-making within the Commercial team.

Lead the biostatistics efforts for clinical studies, providing technical guidance, statistical analysis, and overseeing CRO teams while ensuring regulatory compliance.

The Executive Director of GMP Quality Assurance oversees the GMP QA strategy, ensuring compliance with global regulations, leading a high-performing team, and preparing for regulatory inspections and audits.

Lead design, planning, execution, and quality oversight of clinical trial data management (Phase I-IV). Manage CROs and vendors, ensure EDC/eCRF/ CDM standards, support database locks/snapshots, collaborate with Biostatistics/Programming and other functions, and maintain regulatory-ready documentation for submissions.

The Associate Director oversees CRAs managing CRO monitoring for clinical trials, ensuring compliance, performance, and process development while leading teams and managing training.

The Senior Associate in Regulatory Affairs supports FDA and global regulatory submissions, maintains regulatory data, coordinates with teams, and ensures compliance with submission standards.

The Senior Director of Commercial Strategy will lead the development and execution of the U.S. commercialization roadmap, collaborating with cross-functional teams and managing competitive intelligence processes.

The Associate Director will optimize clinical operations standards, enhance operational efficiency, and manage resources for global clinical trials, ensuring best practices and vendor performance.

Lead the statistical programming function for clinical trials, manage CRO relationships, and mentor team members while driving process improvements and ensuring quality deliverables.

The Clinical Trial Manager oversees global clinical trial programs, ensuring compliance to regulatory standards, managing vendor partnerships, and communicating project statuses while focusing on patient enrollment and data quality.

Manage regulatory project planning and execution for clinical trials, ensuring alignment across teams. Drive submissions and optimize regulatory processes.

The Manager of Clinical Business Operations oversees project planning for clinical programs, ensuring integration of operations, managing resources, and tracking performance metrics.

The Clinical Monitoring Manager oversees in-house CRAs and CROs for clinical trials, ensuring compliance and quality. They manage and support clinical study activities, liaise with stakeholders, and ensure trial readiness.

The Associate Director will lead late-stage development and commercialization of monoclonal antibodies, focusing on process delivery and oversight with CDMO partners.

Manage the end-to-end clinical supply chain for multiple clinical programs, ensuring timely delivery of products while collaborating with various cross-functional teams and maintaining regulatory compliance.

Lead statistical programming for clinical trials, managing programmers and CROs. Oversee programming activities, ensuring timely support for clinical projects and developing programming processes.

The Director of GMP Quality Assurance will ensure quality compliance in biologics manufacturing, oversee audits, manage batch releases, and drive continuous improvement in quality systems.