Global Clinical Project Leader, Partnerships & Delivery

Parexel

Trieste/Trst

In loco

EUR 90.000 - 130.000

Tempo pieno

2 giorni fa
Candidati tra i primi
Generatore di candidature

Una candidatura apposita per questo posto — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

bonus
holiday
pension
other leading-edge benefits

Descrizione del lavoro

Parexel seeks a Clinical Project Leader to guide global studies for Large Pharma partners. You will lead cross-functional teams to deliver trials on time, on budget, and in compliance with ICH GCP, while maintaining high client satisfaction.

This role blends science, project management, and stakeholder engagement in a multinational, collaborative environment. Responsibilities include risk management, budgeting and invoicing oversight, SOP contributions, and study-level client relationships.

Competenze

  • Develop and maintain formal project plans with milestones, budgets, and resources
  • Perform risk management and communicate risks and contingencies to clients
  • Set and ensure quality standards to drive project quality
  • Own and manage client relationships at the study level
  • Oversee project P&L including budgeting, revenue recognition, and invoicing
  • Coordinate cross-functional project teams to complete studies
  • Represent the Project Leadership function in client meetings and presentations
  • Contribute to SOPs and other organizational initiatives
  • Possibly engage in non-billable activities as needed
  • CRO experience with Phase I–III clinical trial project management and demonstrated leadership
  • Oncology essential; Ophthalmology, Neurology, Dermatology or Cardiovascular desirable
  • Strong written and spoken English
  • Financial management and client relationship skills; bid defense experience
  • Pharma experience considered; familiarity with standard business and eClinical systems
  • ICH and GCP knowledge; solid clinical research and protocol design understanding
  • Ability to work in a matrix environment and manage multiple tasks
  • Independent work style with guidance when needed
  • Proactive, solutions-based mindset
  • Critical thinking and problem-solving
  • Excellent interpersonal, verbal and written communication
  • Proficiency in Microsoft Excel, PowerPoint, Word
  • Project planning software
  • Knowledge of eClinical systems

Mansioni

  • Develop and maintain formal project plans with milestones, budgets, and resources
  • Perform risk management and communicate risks and contingencies to clients
  • Set and ensure quality standards to drive project quality
  • Own and manage client relationships at the study level
  • Oversee project P&L including budgeting, revenue recognition, and invoicing
  • Coordinate cross-functional project teams to complete studies
  • Represent the Project Leadership function in client meetings and presentations
  • Contribute to SOPs and other organizational initiatives
  • Possibly engage in non-billable activities as needed
  • CRO experience with Phase I–III clinical trial project management and demonstrated leadership
  • Oncology essential; Ophthalmology, Neurology, Dermatology or Cardiovascular desirable
  • Strong written and spoken English
  • Financial management and client relationship skills; bid defense experience
  • Pharma experience considered; familiarity with standard business and eClinical systems
  • ICH and GCP knowledge; solid clinical research and protocol design understanding
  • Ability to work in a matrix environment and manage multiple tasks
  • Independent work style with guidance when needed
  • Proactive, solutions-based mindset
  • Critical thinking and problem-solving
  • Excellent interpersonal, verbal and written communication
  • Proficiency in Microsoft Excel, PowerPoint, Word
  • Project planning software
  • Knowledge of eClinical systems

Descrizione del lavoro

Parexel seeks a Clinical Project Leader to guide global studies for Large Pharma partners. You will lead cross-functional teams to deliver trials on time, on budget, and in compliance with ICH GCP, while maintaining high client satisfaction.

This role blends science, project management, and stakeholder engagement in a multinational, collaborative environment. Responsibilities include risk management, budgeting and invoicing oversight, SOP contributions, and study-level client relationships.

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