Senior Director – Pharmacovigilance

Emploi pas sur LinkedIn

🕒 il y a 29 jours

🇺🇸 États-Unis – Télétravail

💵 $263 000 - $325 000 / an

⏰ Temps Plein

🟠 Senior

👔 Directeur

👻 Score fantôme 1%

Ce que ça veut dire : la probabilité que personne ne recrute vraiment pour cette offre.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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BBOT

Site WebLinkedInTous les Emplois

51 - 200 employés

🏥 Santé

💼 Conseil

🧬 Biotechnologie

Healthcare • Consulting • Biotechnology

BBOT est une entreprise de biotechnologie développant des thérapies ciblées pour les cancers causés par la signalisation RAS et le PI3Kα. La société se concentre sur la conception rationnelle de médicaments pour inhiber l'état actif ON de RAS et bloquer sélectivement l'activation du PI3K induite par RAS, ciblant plusieurs mutants de KRAS et adoptant de nouvelles approches pour maximiser l'inhibition de la cible. BBOT traduit des décennies de recherche en biologie RAS en candidats thérapeutiques destinés à améliorer les résultats pour les patients atteints de tumeurs causées par RAS et PI3Kα.

Description

• Serve as BBOT’s internal pharmacovigilance subject matter expert and safety medical lead • Provide medical and scientific oversight of safety data across the clinical portfolio • Lead safety surveillance, signal detection, and medical assessment of ICSRs, SAEs, and SUSARs • Chair Safety Review Team meetings and maintain safety monitoring plans, risk-management strategies, and benefit-risk frameworks • Author and review safety content for INDs, IBs, DSURs, annual safety reports, REMS, RMPs, and NDA/BLA safety sections • Represent BBOT in safety-related interactions with FDA, EMA, and other global health authorities • Collaborate on protocol design, informed consent forms, safety stopping rules, dose escalation criteria, and emerging safety signals • Establish and improve the pharmacovigilance system, including adverse-event collection, processing, and reporting workflows • Ensure timely reporting of ICSRs, expedited reports, and aggregate safety reports • Develop SOPs, work instructions, and training materials; lead inspection readiness and serve as PV contact during audits and inspections • Oversee PVAs and SDEAs with CROs, partners, and collaborators • Establish compliance metrics and remediate process, system, and documentation gaps • Support safety database implementation and oversight • Select, onboard, and oversee PV CROs and safety vendors • Manage vendor scopes, performance metrics, governance frameworks, oversight meetings, and quality reviews • Partner with Clinical Operations, Regulatory Affairs, Data Management, and Biostatistics on safety data integration, coding, and reporting • Serve as safety lead on cross-functional program teams and contribute to development plans, risk mitigation, and safety go/no-go decisions • Support DSMB/DMC charters, processes, outputs, safety data packages, and safety narratives • Build BBOT’s pharmacovigilance function, infrastructure, systems, processes, and vendor relationships • Recruit, develop, and lead the PV team as the pipeline grows • Provide pharmacovigilance insights for corporate strategy, pipeline risk, regulatory strategy, and safety go/no-go criteria

🎯 Exigences

• M.D., D.O., or equivalent degree preferred; PharmD or Ph.D. candidates with significant medical safety leadership experience will be considered • Senior Director: minimum 10 years of progressive experience in pharmacovigilance and/or drug safety within the biopharmaceutical industry, with at least 5 years in a leadership or senior lead capacity • Executive Director: minimum 12 years of progressive experience in pharmacovigilance and/or drug safety within the biopharmaceutical industry, with at least 5 years in a senior leadership or function-head capacity • Expertise in safety science and safety operations • Oncology experience required; early-phase oncology experience strongly preferred • Knowledge of FDA 21 CFR Parts 312 and 314, EMA GVP modules, ICH E2A–E2F, and MedDRA/WHO DD coding standards • Experience overseeing PV CROs and safety vendors • Experience authoring and reviewing PV regulatory documents, including DSURs, IB safety updates, IND annual reports, and safety-related submissions • Experience supporting or participating in FDA, EMA, or other health-authority interactions • Familiarity with Argus, Veeva Vault Safety, or ArisGlobal and safety reporting systems • Strong communication and cross-functional collaboration skills • Prior lean, startup, or high-growth biotech experience highly desirable • Executive Director: experience establishing or significantly building a pharmacovigilance function at a lean biotech or as an early PV hire

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