Vice President, Clinical Development

🕒 il y a 2 mois

🇺🇸 États-Unis – Télétravail

💵 $254 900 - $382 300 / an

⏰ Temps Plein

🔴 Expert

👔 Vice-président

🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Precision For Medicine

Precision For Medicine

1001 - 5000 employés

🧬 Biotechnologie

⚕️ Assurance santé

💊 Pharmaceutique

💰 €75 000 000 Private Equity Round en 2015-12

Biotechnology • Healthcare Insurance • Pharmaceuticals

Precision for Medicine est un leader spécialisé dans l’accompagnement du développement et de la mise sur le marché de thérapies innovantes, notamment en oncologie, dans les maladies rares et les maladies auto-immunes. Grâce à une gamme complète de services — gestion d’essais cliniques, services de laboratoire et collecte de biospécimens — l’entreprise intègre des capacités avancées en biomarqueurs ainsi que des solutions de fabrication pour fluidifier des processus de développement clinique complexes. Sa mission est d’accélérer la recherche et d’apporter aux patients des solutions médicales qui changent la vie, en dépassant les inefficacités traditionnelles souvent observées dans le paysage du développement pharmaceutique.

Description

• Reports to Chief Medical Officer, and across Precision for Medicine, supporting medical strategy. • Provides medical and strategic support for business development activities globally including client engagement, proposal support, client capabilities meetings, and professional meetings. • Provides strategic drug development consulting to autoimmune, rare and orphan disease clients. The consulting will be provided in the context of an integrated strategy with medical, clinical, regulatory, biostatistical, translational and marketing insights. • Create, review, or revise protocols, case report forms, training materials, project-specific tools, analysis plans, study designs, clinical trial reports, and investigational new drug applications. • Review laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed. • Participate and drive feasibility discussions relating to specific project proposals. • Develop training modules and conducts training for project teams and colleagues as necessary. • Ensure high quality, data driven deliverables that meet the highest standards of medical, ethical, and scientific integrity and conduct. • Propose strategies to manage and accelerate timelines for drug development strategies. • Ensures customer satisfaction by working closely with senior management, PFM operations, to provide optimum strategic consultancy to clients.

🎯 Exigences

• Successful completion of MD, MBBS, or equivalent training plus completion of training including a fellowship (Endocrinology, Rheumatology, Hematology-Oncology or other related field, board certification preferred, including European equivalents). • Experience in direct interactions with US and/or EU Regulatory Authorities • At least 10 years of senior leadership experience in the clinical research industry with a demonstrated knowledge and substantial experience including related disciplines (i.e. operations, medical monitoring, biostatistics, regulatory, preclinical, translational pharmacology, etc.) Or equivalent combination of education, professional training and experience that provides the individual with the required knowledge, skills, and abilities to perform the job.

🏖️ Avantages

• This role is also eligible for a discretionary annual bonus • health insurance • retirement savings benefits • life insurance and disability benefits • parental leave • paid time off for sick leave and vacation

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