Feasibility Manager

🕒 il y a 20 jours

🌐 Hongrie, Royaume-Uni, +5 autres pays – Distant

🇭🇺 Hongrie – Télétravail 🇬🇧 Royaume-Uni – Télétravail 🇪🇸 Espagne – Télétravail 🇵🇱 Pologne – Télétravail 🇷🇴 Roumanie – Télétravail 🇷🇸 Serbie – Télétravail 🇸🇰 Slovaquie – Télétravail

⏰ Temps Plein

🟢 Junior

🟡 Intermédiaire

🧪 Chercheur Clinique

👻 Score fantôme 20%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.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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Precision For Medicine

Site WebLinkedInTous les Emplois

1001 - 5000 employés

🏥 Santé

💼 Conseil

📦 Logistique

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

Healthcare • Consulting • Logistics

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

• Lead or contribute to feasibility assessments for client requests for proposals • Review clinical protocols, study assumptions, client information, and operational plans for United States and global clinical trials • Conduct and synthesise competitive landscape, historical recruitment, standard-of-care, treatment landscape, epidemiology, country, site, and patient-pool analyses • Translate evidence into clear country, site, enrolment, and operational recommendations • Develop logical, transparent rationales for assumptions and identify important data limitations and feasibility risks • Present feasibility methods, findings, recommendations, and supporting rationale to Business Development colleagues, proposal teams, and clients • Collaborate with internal colleagues, external consultants, data partners, investigators, and sites to gather and interpret feasibility information • Plan, coordinate, and analyse targeted site and investigator outreach, as appropriate • Participate in bid-defence meetings and client discussions • Contribute to the continued development of feasibility methods, data sources, tools, templates, and best practices • Share knowledge and support the development of colleagues within the Feasibility team • Work effectively across functions, therapeutic areas, and geographic regions • Contribute to initiatives that strengthen Precision for Medicine’s scientifically driven approach and client offering

🎯 Exigences

• Bachelor’s degree in life sciences or a related discipline • At least two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related area • Experience conducting or contributing to clinical trial feasibility analysis and site or country identification • Ability to interpret clinical, scientific, epidemiological, and operational information and develop clear recommendations • Professional proficiency in written and spoken English • Equivalent combinations of education, qualifications, and relevant experience may be considered • Strong analytical and critical-thinking skills, with the ability to synthesize multiple evidence sources • Ability to develop and communicate a clear rationale for feasibility assumptions and recommendations • Strong attention to detail while maintaining awareness of the overall study strategy • Ability to manage multiple concurrent deliverables, stakeholders, priorities, and deadlines • Excellent written, verbal, and presentation skills • Advanced proficiency in Microsoft Excel, PowerPoint, and Word • Confidence working with web-based data, intelligence, and analytics platforms • Strong ownership of deliverable quality, accuracy, and timeliness • Collaborative working style and ability to operate effectively in a matrix environment • Ability to work independently while seeking input and escalation appropriately • Working knowledge of ICH-GCP principles • Preferred: postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline • Preferred: experience supporting global clinical trials • Preferred: experience in oncology, rare disease, or other complex clinical-development programs • Preferred: experience presenting analyses and recommendations to clients or senior stakeholders • Preferred: familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms

🏖️ Avantages

• Fully remote work in eligible countries • Opportunity to contribute to complex clinical programs in oncology and rare diseases • Opportunity to work with clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences • Equal Opportunity Employer • Reasonable accommodation available during the application process