For Pharma

Oncostrata medical monitors and clinical development scientists are ready to effectively integrate and collaborate closely with your cross-functional teams, supporting your ongoing clinical development programs with our oncology and hematology expertise.

Clinical Development Expertise

Provide clearly articulated scientific explanations and presentations to multi-disciplinary teams and stakeholders

Medical data review support (e.g. prior to database snapshots or interim/final analysis)

CRO oversight

Contribution to submission documentation (e.g. Clinical Study Reports, Safety Narratives)

Clinical trial documentation authoring (e.g. Clinical Study Protocol, IB, ICF)

Review of Tables, Listings, and Figures

Assists in safety evaluation, trend assessment, and preparation for IDMC meetings

Scientific publication authoring assistance

Investigational New Drug Applications and Biologics License Applications

Clinical landscape evaluation and expansion into new disease areas

Literature review and competitive landscape

Anti-tumor efficacy assessments, indication-specific, for solid tumors and hematologic malignancies (examples: based on Lugano classification, RECIST 1.1, RANO, iwCLL, NCCN guidelines, etc.)