Associate Director, Drug Safety and Pharmacovigilance

🕒 Maio 21

Candidatar-se

Encontrar Vagas Remotas Similares

Configurar Alerta de Email para Novas Vagas

📊 Verifique sua pontuação de currículo para esta vaga

Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

Enviar Currículo

Celcuity

SiteLinkedInTodas as Vagas

51 - 200 funcionários

🏥 Saúde

🏭 Manufatura

🧬 Biotecnologia

🔥 Investimento no último ano

💰 $500.000.000 Post-IPO Debt - Celcuity em 2025-09

Healthcare • Manufacturing • Biotechnology

A Celcuity é uma empresa de biotecnologia em estágio clínico que desenvolve terapias direcionadas para bloquear de forma abrangente a via PI3K/AKT/mTOR (PAM) no tratamento de múltiplos tumores sólidos. Seu principal candidato a produto, o gedatolisibe, é um potencial inibidor pan-PI3K e mTORC1/2 de primeira classe em desenvolvimento clínico avançado (incluindo ensaios de Fase 3 VIKTORIA) para câncer de mama avançado HR+/HER2- e outras indicações, como câncer de próstata. A empresa avança com um pipeline focado em inibidores da via PAM, publica dados clínicos, envolve-se com investidores e reguladores, e tem como missão melhorar os resultados para pacientes com câncer.

Descrição

• Provide leadership and oversight of external safety vendors to ensure high‑quality, timely, and compliant execution of all outsourced safety activities. • Lead the preparation, authorship, and review of aggregate safety reports (e.g., DSURs, PADERs, line listings) and manage associated timelines and cross‑functional inputs. • Provide day-to-day direction to the Safety Operations team and communicate program-level updates to internal and external stakeholders. • Demonstrate initiative by exploring potential solutions and offering thoughtful recommendations, engaging leadership when additional insight or alignment is needed. • Oversee the review and assessment of adverse event reports for assigned programs, ensuring appropriate follow‑up and timely expedited reporting in accordance with global regulatory requirements. • Contribute to the development, implementation, and continuous improvement of SOPs, work instructions, templates, and systems to ensure compliance with global clinical trial regulations and industry best practices. • Ensure procedural deviations are documented, investigated, and addressed through effective corrective and preventive actions. • Support inspection readiness activities and serve as a key contributor during audits and global health authority inspections. • Develop and maintain study‑specific safety management plans and related documents, ensuring clear delineation of responsibilities between Celcuity and CRO partners. • Ensure adherence to Safety Data Exchange Agreements and compliance with all agreed‑upon reporting requirements and timelines. • Review and provide expert input on safety-related sections of clinical documents, including protocols, charters, Investigator Brochures, and Informed Consent Forms. • Develop, monitor, and interpret key performance indicators and metrics for internal teams and external vendors to evaluate performance and drive continuous improvement. • Serve as the safety subject matter expert for internal teams and external stakeholders, providing guidance on safety operations, regulatory expectations, and best practices. • Perform other tasks as required to assist in company and departmental activities.

🎯 Requisitos

• 10+ years of drug safety/pharmacovigilance experience within a sponsor environment or a combination of sponsor and CRO roles. • Bachelor’s or advanced degree in a life science or healthcare‑related discipline (e.g., MD, RN, PharmD, NP, PhD, MPH). • Comprehensive knowledge of global clinical safety regulations, guidelines, and industry best practices. • Extensive experience working with commercial safety databases (Argus or ARIS-G), electronic data capture systems, and trial master files. • Demonstrated experience preparing aggregate safety reports for investigational and/or marketed products (e.g., DSURs, PSUR/PBRERs, PADERs) and contributing to IB updates. • Strong knowledge of MedDRA and WHODrug coding conventions. • Excellent written and verbal communication skills, with the ability to convey complex information clearly and concisely. • Strong interpersonal skills with the ability to collaborate effectively across functions and organizational levels. • Exceptional attention to detail and ability to manage multiple priorities and documentation requirements. • Strong technical and analytical skills with advanced proficiency in MS Office (Word, Excel, PowerPoint). • Ability to work independently or collaboratively, demonstrating sound judgment and decision‑making in a fast‑paced environment. • Naturally takes initiative, contributing to continuous improvement efforts and proactively identifying opportunities to enhance processes within the department. • Continuous improvement mindset with a focus on innovation, efficiency, and operational excellence. • Flexible, adaptable, and committed to maintaining a positive and professional demeanor.

🏖️ Benefícios

• Medical insurance • Dental insurance • Vision insurance • 401(k) match • PTO • Paid holidays • Annual performance incentive bonus • New hire equity package