Project Director

🕒 il y a 1 mois

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

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

⏰ Temps Plein

🔴 Expert

👔 Directeur

👻 Score fantôme 13%

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 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

• Serve as primary client point of contact and participate in proposal activities and client presentations • Oversee all aspects of clinical research trials and assigned portfolios • Direct project managers through project establishment, planning, initiation, procurement, execution and closeout • Manage study budgets, scope, change orders and project profitability • Oversee billable hours, billing compliance and forecasting • Develop or oversee comprehensive project plans, timelines, risk management and mitigation strategies • Ensure quality management, eTMF inspection readiness, quality notifications and CAPA plans • Establish tracking metrics for trial and team progress • Prepare project status updates, KPI reports and presentations for clients and senior management • Lead internal and client meetings and drive study-level strategies • Oversee cross-functional project teams and trial execution • Communicate protocol and study issues and implement corrective actions • Conduct formal presentations, including bid defenses • Ensure study-specific training and compliance • Support business development and marketing activities, including bid defense travel • Mentor associate, project and senior project managers • Contribute to departmental updates and company SOP development • Provide ongoing feedback and annual performance reviews for functional team members • Identify project-level performance problems and ensure corrective action • Complete training, time reporting and administrative duties • Perform other duties assigned by management

🎯 Exigences

• Degree or equivalent combination of education/experience in science or health-related field for EU candidates; advanced degree preferred • Minimum of 8 years of clinical research experience or proven competencies for the position • Minimum of 5 years of direct project management experience • Highly proficient with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC and CTMS • Excellent communication and interpersonal skills • Excellent organizational skills, attention to detail, and customer service demeanor • Experience managing highly complex and global studies or a portfolio of studies • Mastery of ICH-GCP and relevant Precision SOPs • Excellent knowledge of project management techniques and tools • Highly experienced in cross-functional project management environments • Strong understanding of cross-functional management • Strong understanding of project planning, risk management and change management • High level of integrity and professional and ethical standards • Ability to lead and inspire study teams • Demonstrated excellence in time management, negotiation, critical thinking, decision making, analytical, presentation, verbal and written communication skills • Expert understanding of project management software • Highly experienced in pharmaceutical and/or device research • Expertise in strategic planning, risk management and change management • Highly developed customer orientation, influence, negotiation and conflict management skills • Ability to work and plan independently and in a team environment • Ability to travel domestically and internationally, including overnight stays

🏖️ Avantages

• Supportive and collaborative environment • Work-life balance • Team development encouragement • Equal Opportunity Employer • Reasonable accommodation available for applicants with disabilities