Clinical Project Leader – Partnerships

🕒 il y a 1 mois

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

💰 Responsable de comptes

🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Parexel

Parexel

10 000+ employés

Fondée en 1983

💼 Conseil

🏥 Santé

📦 Logistique

💰 Venture Round en 1990-01

Consulting • Healthcare • Logistics

Parexel est l'une des plus grandes organisations de recherche clinique (CRO) au monde, fournissant des services complets pour le processus de développement clinique de la Phase I à IV. L'entreprise se spécialise dans la gestion de portefeuille, la gestion des essais cliniques, la stratégie réglementaire, l'accès au marché et la gestion du cycle de vie des produits biopharmaceutiques. Parexel vise à accélérer la mise sur le marché de médicaments qui changent la vie en tirant parti de son expertise clinique, réglementaire et thérapeutique. Avec une équipe mondiale de plus de 21 000 professionnels, Parexel s'efforce d'intégrer les perspectives des patients et des conceptions d'essais innovantes pour développer des traitements dans des domaines thérapeutiques tels que l'oncologie, les neurosciences, les maladies rares et plus encore. Elle se concentre sur la fourniture d'essais cliniques centrés sur le patient et efficaces.

Description

• Lead project delivery for Large Pharma Partnership clients and their projects globally • Actively lead Parexel and client teams using clinical research expertise and client insight • Provide cross-functional leadership for clinical trials, studies and project teams • Deliver projects on time, within budget, at high quality and in compliance with ICH GCP • Develop and maintain formal project plans covering milestones, budgets and resources • Identify project risks, implement contingency plans, mitigate risks and keep clients informed • Establish project quality standards and ensure first-time quality of deliverables • Own study-level client relationships and communications • Manage project P&L, budgets, revenue recognition, forecasting, resources, pass-through costs, scope changes and invoicing • Manage cross-functional project teams and enable successful study completion • Represent Project Leadership in client meetings and presentations, including bid pursuit and investigator meetings • Review SOPs and lead or contribute to organizational initiatives

🎯 Exigences

• Bachelor’s degree or equivalent level of education; Science or Medical related field preferred • Proven substantial clinical project management experience may substitute for the educational level • Advanced degree desirable • Strong previous CRO experience • Understanding of Phase I, II-III clinical trial project management • Demonstrable project leadership skills • Oncology therapeutic area expertise essential • Ophthalmology, Neurology, Dermatology or Cardiovascular experience desirable • Strong command of written and spoken English essential • Strong financial management and client relationship skills • Involvement with bid defense activities • Familiarity with standard business and eClinical systems used in Clinical Research desirable • Knowledge of ICH and GCP regulations in relevant geographies • Solid clinical knowledge and understanding of clinical research and protocol design • Proactive, solutions-based approach • Critical thinking and problem-solving • Excellent interpersonal, verbal and written communication skills • Strong client focus and accountability • Ability to manage multiple and varied tasks, prioritize workload and maintain attention to detail • Ability to work in a matrix environment and collaborate with teams • Basic understanding of the project life cycle • Ability to work independently with oversight guidance • Proficiency in Microsoft Excel, PowerPoint, Word and project planning software

🏖️ Avantages

• Structured career pathway and development within the role • Competitive salary • Bonus • Car allowance (country specific) • Benefits package including holiday, pension and other leading-edge benefits

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