Vice President, Clinical Development; Oncology

Corbus is recruiting a Vice President, Clinical Development. This is a senior role focused on a company's clinical development, scientific strategy, and medical affairs. The Vice President, Clinical Development role involves leading clinical programs, ensuring scientific and regulatory compliance, and collaborating across teams to develop therapies. This role provides scientific expertise necessary to design, implement and interpret data from clinical studies.

The role provides scientific input and oversight, as well as leadership and management of cross‑functional execution of clinical studies in collaboration with Clinical Operations. This role will be responsible for the scientific aspects of global clinical trial delivery including protocol design and writing, analysis of data, management and reporting of trials in accordance with company plans/objectives, ICH‑GCP, country requirements and company standard operating procedures.

Specifically, this includes writing and/or reviewing protocols, interacting with sites for feasibility assessment, supporting site selection, data review and writing/reviewing the clinical study report, for one or more clinical trials. This role will support planning, publication strategy and other tasks. This role provides scientific and operational expertise to ensure patient safety in clinical studies and effective communication of safety to regulatory and ethical bodies.

This role works to analyze, summarize and report on safety data. Develops cumulative safety update reports and ensures compliant report of individual safety reports to regulatory bodies and ethical committees. The Vice President, Clinical Development is a qualified physician scientist with exceptional academic clinical trials' experience in Oncology development. They will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late‑Stage portfolio.

The Vice President, Clinical Development will play a pivotal role in further growing the Clinical Development function at Corbus Pharmaceuticals and leading and contributing to the unique science. This role will offer you a high level of influence and impact on novel therapies by partnering externally with some of the world’s leading clinicians in the field of Oncology while collaboratively partnering with our Clinical Development Organization at Corbus Pharmaceuticals.

In this position, the Vice President, Clinical Development provides critical analysis of safety data and translates complex scientific information into clear, compliant, and well‑structured reports and documentation for senior leadership (including the CMO) and regulatory agencies.

• Leads and/or participates in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input and guidance. Includes contributing to and reviewing of clinical protocols
• Gathers, analyzes and summarized data and information necessary to create the CD plan. May also delegate such research and analysis to less experienced Clinical Scientists
• Maintains scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment and participates in competitive intelligence assessments
• Represent Clinical development in collaboration with Research and Translational Sciences for alignment on biomarker strategy and pharmacological assessments Clinical Development Plan Implementation
• Reviews and/or writes additional clinical science documentation and/or clinical science input into other documentation managed by Corbus Pharmaceuticals (e.g., protocol summaries, safety monitoring plans, process documents, investigator brochures, etc.)
• Supports with completion and submission of regulatory filings and other regulatory documentation
• Oversees the review, analysis and reporting of clinical data in collaboration with biometrics and data management to enable clinical decision making and regulatory filings
• As needed/appropriate, collaborates with others in the review of safety narratives and other safety‑related guidelines and…