Ocugen Jobs in United States

+The Principal Statistical Programmer is a key member of Ocugen’s clinical operations team. · +Ensures the accurate programming of data extracts and data displays · Develops Macro repository for creation of datasets, conducting analyses, and formatting results into TFLs · Create ...

Senior Manager / Associate Director Regulatory Operations · Ocugen seeks a Senior Manager / Associate Director to lead regulatory operations and submissions across global programs. · Lead cross-functional teams to prepare regulatory documents · Description: · The role will overs ...

Ocugen is a biopharmaceutical company seeking an Environmental Health and Safety Manager to build and lead site-specific EHS standards and programs. · ...

The Senior Manager / Associate Director of Regulatory Operations will lead the planning preparation and execution of regulatory submissions to advance Ocugen's biologics cell and gene therapy programs. · This role provides strategic and operational leadership for global regulator ...

The Principal Clinical Data Manager provides strategic leadership and oversight of clinical data management activities across multiple programs. This role manages a team of data managers, ensuring high-quality data collection, transformation, and submission in compliance with reg ...

Job Purpose · The Senior Document Control Specialist is responsible for managing GxP-controlled documentation supporting Manufacturing and Quality Control (QC) operations using the Veeva Quality Suite. This role ensures documents are accurate, current, compliant, and inspection-r ...

Senior Document Control Specialist · The Senior Document Control Specialist is responsible for managing GxP-controlled documentation supporting Manufacturing and Quality Control (QC) operations. · Serve as a Veeva Quality Docs subject matter expert providing guidance on system us ...

Job Summary · The Principal Statistical Programmer will lead and oversee programming activities for clinical trial data analysis and global regulatory submissions. · Duties and Responsibilities: · Set and own the statistical programming strategy across multiple clinical studies a ...

The Principal Biostatistician is a key member of Ocugen's clinical development team. · This individual will be responsible for providing statistical services including analysis, interpretation, design, and reporting or communication of data evidence for research, development, and ...

The project manager will assist in the planning and execution of various product developmental programs from pre-clinical through commercialization with a specialization of -regulatory operations (Phase 1-3) while adhering to schedule, scope, and budget requirements. · ...

The Senior Document Control Specialist is responsible for managing GxP-controlled documentation supporting Manufacturing and Quality Control (QC) operations using the Veeva Quality Suite. · This role ensures documents are accurate, current, compliant, and inspection-ready, · supp ...

The Principal Programmer will lead and oversee programming activities for clinical trial data analysis and global regulatory submissions. · ResponsibilitiesSet and own the statistical programming strategy across multiple clinical studies. · Oversight of SDTM, ADaM, and analysis p ...

The Associate Director of Regulatory Affairs - Gene Therapy will support the development and execution of regulatory strategy for Ocugen's gene therapy portfolio. · Contribute to the design and execution of global regulatory strategy for Ocugen's gene therapy programs. · Collabor ...