Search the 8 jobs at Apellis Pharmaceuticals

The Field Reimbursement Manager minimizes access and reimbursement barriers for patients and providers in Ophthalmology. They work with customers to resolve complex reimbursement issues, provide education on support programs, and coordinate across teams to enhance patient accessibility to Apellis products.

The Scientist will conduct sample preparation and analysis for pharmacology studies, develop biomarkers for neurologic and ocular diseases, communicate results, and contribute to experimental designs and assay development, while ensuring compliance with documentation practices.

The HRIS Senior Analyst is responsible for managing and optimizing Workday functionalities including reporting, analytics, and configuration. Key tasks involve troubleshooting issues, creating reports and dashboards, executing test scenarios, and collaborating with stakeholders to meet business requirements.

The Accounting Manager will oversee the general accounting function for North America, manage the month-end close process, review and prepare journal entries and account reconciliations, and ensure compliance with accounting standards. This role includes coaching staff accountants, managing variances, and improving accounting processes.

Field Reimbursement Manager responsible for optimizing access to Apellis' Ophthalmology portfolio by addressing access barriers and providing education and support on reimbursement support programs. Collaborates with internal and external stakeholders to address patient and practice reimbursement issues. Requires a Bachelor's degree and 10 years of commercial experience in the pharmaceutical industry.

The Field Reimbursement Manager (FRM) is responsible for addressing access barriers for patients and providers to optimize access to Apellis' Ophthalmology portfolio. They partner with internal and external stakeholders to identify and address patient and practice reimbursement issues, educate facility staff, provide coverage information, and support patient drug accessibility. The FRM also maintains compliant relationships with relevant societies and stays updated on industry trends.

The Principal Scientist will manage and oversee non-clinical and clinical biomarker bioanalysis, including method development, validation, and interactions with specialty labs. Responsibilities include collaboration with cross-functional teams, maintaining quality assurance, and contributing to the development of novel therapeutics. This role requires a strong background in bioanalytics, laboratory management, and the drug discovery process.

The Research Scientist will lead projects focused on glaucoma and the complement system, managing external collaborations, optimizing therapeutic targets, and contributing to drug development. Responsibilities include project management, data presentation, and teamwork across functions.