Feasibility Manager

🕒 il y a 1 jour

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

🇬🇧 Royaume-Uni – Télétravail 🇪🇸 Espagne – Télétravail 🇭🇺 Hongrie – 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.

Postuler Maintenant

Trouver des Emplois à Distance Similaires

Configurer une alerte email pour les nouveaux emplois

📊 Vérifiez votre score de CV pour ce poste

Améliorez vos chances d'obtenir un entretien en vérifiant votre score de CV avant de postuler.

Télécharger le CV

Precision Medicine Group

Site WebLinkedInTous les Emplois

1001 - 5000 employés

Fondée en 2012

💼 Conseil

🏥 Santé

📦 Logistique

💰 €35 200 000 Venture Round en 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group est un groupe mondial d’experts spécialisé dans la médecine de précision, qui combine sciences de laboratoire avancées, informatique translationnelle, affaires réglementaires, insights payeurs et communication marketing. L’entreprise se consacre à lever les défis de développement produit et de mise sur le marché pour des clients des secteurs pharmaceutique et des sciences de la vie. Ses services incluent une R&D orientée par les biomarqueurs, ainsi qu’un accompagnement à la commercialisation pour les organisations des sciences de la vie, du lancement jusqu’à la maturité du produit. Precision Medicine Group opère via deux pôles principaux : Precision for Medicine et Precision AQ, spécialisés respectivement dans les solutions cliniques et commerciales.

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 arrangement • Opportunity to contribute to complex oncology and rare-disease clinical programs • Opportunity to support meaningful therapies for patients • Equal opportunity employment • Reasonable accommodation during the application process