Robert Mo Email & Phone Number

Greater Boston

Greater Boston

Led drug product programs to achieve clients' project deliverables, and implemented new processes to improve business practices. Served as account/project manager or FTE consultant to collaborate with clients and execute their timelines and goals. Generated new business opportunities and marketing content for small molecule development and manufacturing services.

Cambridge, Ma

Led drug product development and manufacturing team for clinical and commercial supply. Developed and executed Vafseo® (vadadustat) drug product registration objectives, budget and timelines for formulation development, process development, scale-up and technology transfer activities. Managed multiple contract development and manufacturing organizations (CDMOs). Represented CMC in meetings and communications with internal/external cross-functional stakeholders, regulatory health authorities and strategic commercial partners. Authored source documents and regulatory filings.

Cambridge, Ma

Led drug product development and manufacturing team for clinical supply. Developed and executed Vafseo® (vadadustat) drug product registration objectives, budget and timelines for formulation development, process development, scale-up and technology transfer activities. Managed multiple contract development and manufacturing organizations (CDMOs). Represented CMC in meetings and communications with internal/external cross-functional stakeholders, regulatory health authorities and strategic commercial partners. Authored source documents and regulatory filings.

Cambridge, Ma

Served as formulation project leader for discovery and clinical programs. Responsibilities included developing oral/parenteral formulations, authoring regulatory CMC pharmaceutical development sections, identifying and addressing biopharmaceutical risks, and coordinating multi-disciplinary activities among functional groups for preclinical, toxicology and clinical studies.

Groton, Ct

Served as formulation project leader for discovery and clinical programs. Responsibilities included developing oral/parenteral formulations, authoring regulatory CMC pharmaceutical development sections, identifying and addressing biopharmaceutical risks, and coordinating multi-disciplinary activities among functional groups for preclinical, toxicology and clinical studies.

Irvine, Ca

- Developed encapsulated drug formulations for dermal application.- Established physicochemical measurement methods to differentiate and select a formulation of choice.- Provided formulation recommendation based on the results of physicochemical characterization and in vitro/in vivo studies.

Los Angeles, Ca

Dissertation Title: Cell Penetrating Peptide-based Polyplexes for siRNA Delivery- Designed cell penetrating peptide-based siRNA delivery systems.- Compared cationic and amphipathic cell penetrating peptides for siRNA delivery and efficacy.- Identified a correlation between lipid- and cell penetrating peptide-based siRNA transfections and increased intracellular presence of autophagosomes.

Summit, Nj

Developed a controlled release matrix tablet of a poorly soluble drug for once-a-day dosing using hot melt extrusion technology.

Doctor Of Philosophy (Ph.D.), Pharmaceutical Sciences

Bachelor Of Science (Bs), Biomedical Engineering

Student, Extension Studies - Finance

Education record

Education record