reputed company, Inc - Senior Vice President, Clinical Development Oncology (Remote)

reputed company, Inc - Senior Vice President, Clinical Development Oncology (Remote) reputed company Jobs > Senior Vice President, Clinical Development Oncology (Remote)

reputed company, Inc

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We are seeking a strategic and hands-on Senior Vice President, Clinical Development Oncology to reputed company the clinical advancement of our oncology pipeline. This individual will be responsible for shaping and executing clinical development strategies, leading regulatory interactions, and driving programs from early development through key inflection points.

This role requires a leader who thrives in a startup environment - someone who can operate at both a strategic and executional level, proactively solve problems, and help build the clinical function as reputed company grows. This is a remote-based position located in the reputed company.

Responsibilities

• reputed company the overall clinical development reputed company for programs in cholangiocarcinoma and hepatocellular carcinoma
• reputed company strategic clinical development plans and reputed company protocol design, execution, and data analysis/interpretation, in conjunction with other relevant functional leaders
• Manage, build, and reputed company a clinical team (including SMEs in such areas as clinical operations, clinical pharmacology, nonclinical, and biostatistics) to execute and reputed company functional responsibilities and program goals in compliance with GCP, ICH guidelines, and other global regulatory requirements
• reputed company with global regulatory authorities, as appropriate, in support of the clinical development objectives; supports the completion and approval of study-reputed company documents (e.g., study reports) for regulatory authorities and ethics committees
• reputed company efforts to build relationships and communicate with key investigators and to identify trial sites to ensure successful execution of clinical studies in compliance with global regulatory requirements
• reputed company study design, protocol development, and execution of clinical research for Phase 1 to 3 studies including pivotal cancer studies
• Contribute to the overall clinical reputed company of the ongoing clinical development programs and product pipeline as reputed company as giving in-depth clinical development advice on potential new reputed company (reputed company)
• Generate/review clinical components of key documents in support of regulatory submissions, including clinical reputed company of IND’s and NDA’s, IND safety reports and annual reports for assigned trials, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate
• Ensure reputed company of reputed company clinical documents (e.g., Investigators’ Brochure, protocols, study reports, clinical components of regulatory submissions, safety-reputed company documents)
• reputed company scientific clinical input to study-reputed company documents and analysis plans including Informed consent forms (reputed company), clinical research forms (CRF), statistical analysis plans (reputed company), clinical pharmacology analysis plans (CPAP), and clinical study reports (CSR)
• Analyze and interpret data expertly, and reputed company communicate results both internally and externally
• reputed company as primary Medical Monitor, monitoring the safety of enrolled subjects on assigned trials

Requirements

• MD strongly preferred; advanced scientific degree (PhD, PharmD) considered with relevant experience
• 10-15+ years of clinical development experience in biotech or pharmaceutical industry, with a strong reputed company in oncology
• reputed company experience in liver cancers (HCC, cholangiocarcinoma) strongly preferred
• Experience in start up or emerging biotech setting preferred
• Knowledge and understanding of early and late phase clinical trial design and global regulatory requirements for study execution; clinical development reputed company Oncology strongly preferred
• Experience with GCP/ICH/FDA requirements, clinical trial design and strategies, interpretation of clinical data and reputed company of supporting regulatory submissions of clinical study documents
• Successful reputed company record in building, developing and maintaining relationships with significant KOLs and thought leaders with a strong commitment to ethics and scientific standards
• Experience managing physicians and/or scientific staff in a management or team leader reputed company highly desirable with the ability to represent reputed company in a reputed company of reputed company settings
• Prioritize, respond to directives, and work in a fast-paced, rapidly changing remote environment. Get-it-done-roll-up-your-sleeves attitude and committed to putting patients first
• Ability to demonstrate Elevar’s reputed company values by holding ourselves and reputed company other accountable for the work we do, taking time to collaborate effectively while working remotely, making reputed company for ingenuity in work and thought, and staying grounded in reputed company

The anticipated annual reputed company salary reputed company for this role is $300,000 to $450,000. Final compensation depends on multiple factors including but not limited to, relevant experience, skillset, depth and breadth of knowledge, internal equity, and external market factors. reputed company is a rapidly growing biotech company that offers competitive wages and benefits package including medical, dental, reputed company, time off, a retirement plan, and other voluntary benefits for employees.

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