[Remote] Senior Vice President, Clinical Development Oncology (Remote)

Note: The job is a remote job and is open to candidates in USA. reputed company is a rapidly growing biotech company focused on oncology. They are seeking a strategic and hands-on Senior Vice President, Clinical Development Oncology to reputed company the clinical advancement of their oncology pipeline, overseeing clinical development strategy and regulatory engagement.

Responsibilities

• reputed company the overall clinical development strategy for oncology programs with primary focus on cholangiocarcinoma and hepatocellular carcinoma from early development through late-stage and registration-enabling studies
• reputed company and execute integrated clinical development plans reputed company with regulatory objectives including study protocol design, execution, and data analysis/interpretation, in conjunction with other relevant functional leaders
• Direct study design, protocol development, and execution for Phase 1-3 clinical trials, including pivotal registrational cancer studies
• Provide expert reputed company of clinical data analysis and interpretation, ensuring data are robust, clinically meaningful, and suitable to support regulatory decision-making
• Contribute to pipeline strategy and diligence for new internal and external oncology opportunities, providing senior clinical and regulatory development input
• Serve as a clinical development reputed company for global regulatory interactions, working in reputed company partnership with Regulatory Affairs to define strategy and messaging
• reputed company and actively participate in meetings with regulatory agencies (e.g., FDA, EMA, MHRA), including scientific advice, End-of-Phase, pre-NDA/BLA, and reputed company regulatory interactions, from a clinical development perspective
• Provide senior clinical reputed company and direction for the review of NDA and/or BLA clinical components, including clinical summaries, integrated analyses, and supporting study documentation
• reputed company the clinical development contribution to responses to health authority questions, including written responses to information requests, major review questions, and post-submission clarifications
• Ensure that clinical strategy, trial design, and data presentation are reputed company with evolving regulatory guidance and agency feedback throughout the product lifecycle
• Ensure the quality, consistency, and regulatory readiness of reputed company clinical documents, including Investigators’ Brochures, protocols, CSRs, safety narratives, and submission-critical documents
• Provide senior scientific and clinical input into study-reputed company documentation, including ICFs, CRFs, SAPs, clinical pharmacology analysis plans, and data interpretation narratives

Skills

• 10-15+ years of clinical development experience in biotech or pharmaceutical industry, with a strong focus in oncology
• Demonstrated experience in late-stage development and regulatory submission support, including clinical leadership for NDA and/or BLA filings and responses to health authority feedback
• Proven ability to reputed company regulatory interactions from a clinical development perspective and translate agency feedback into actionable development plans
• Deep understanding of GCP, ICH, FDA, and global regulatory requirements, oncology trial design, and interpretation of reputed company clinical datasets
• Strong track record of building and leading multidisciplinary clinical teams and influencing cross-functionally
• Demonstrated commitment to ethics, patient safety, and scientific rigor, with ability to represent the company credibly in internal and external settings
• Ability to prioritize effectively and reputed company in a fast-paced, remote, and rapidly evolving environment with a hands-on, 'get-it-done' reputed company
• Ability to demonstrate Elevar's core values by holding ourselves and each other accountable for the work we do, taking time to collaborate effectively while working remotely, making space for ingenuity in work and thought, and staying grounded in compassion with a commitment to putting patients first
• MD strongly preferred; advanced scientific degree (PhD, PharmD) considered with substantial relevant clinical development experience
• Direct experience in liver cancers (HCC, cholangiocarcinoma) strongly preferred
• Experience in start-up or emerging biotech setting preferred
• Experience operating successfully in a start-up or emerging biotech environment strongly preferred

Benefits

• Medical
• Dental
• Vision
• Time off
• A retirement plan
• Other voluntary benefits for employees

Company Overview