Clinical Project Manager

il y a 2 semaines


Bruxelles, Région de Bruxelles, Belgique Amador Bioscience Temps plein

Position Summary
The Clinical Project Manager is responsible for providing direct oversight, management, and follow-up on assigned projects.

He/she will be responsible for all aspects of clinical trial-related support, including but not limited to, coordination of statement of work (SOW), invoicing, budget tracking, day-to-day operational support, status reports, relationship review with clients, and regular update to senior leadership.


Key Responsibilities

  • Manages the delivery of all technical and service aspects of projects and studies for clients.
  • Determines the preliminary design of the study and evaluates and understands the study.
  • Responsible for the organization, implementation, and schedule management of clinical projects.
  • Provide internal and external Clients with a central point of contact for projects. Ensures that all key stakeholders are knowledgeable of project milestones, plans, program status, and decisions through regular reporting and communication.
  • Assist with study contracting and accountable for tracking costs vs. budget, budget forecasting and planning.
  • Initiates the involvement of appropriate functions / CRO, maintaining continuous communication with those functions / CRO, and ensures the work delivered to customers is of a consistently high standard.
  • Negotiate with both internal and external Clients with strong interpersonal skills.
  • Other assigned responsibilities that are related to Amador Bioscience's business.

Qualifications and Education Requirements

  • Bachelor's, Master's or equivalent industry experience in a relevant technical discipline such as life science, biology, and etc. A minimum of 5 years in the pharmaceutical or biotechnology industry including Contract Research Organization (CRO) or other clinical trials environment; at least 3 years of relevant Project Management experience.
  • Strong research, analytical, criticalthinking, and problemsolving skills.
  • Proven ability to motivate and manage cross functional project teams. A minimum of Two (2) years' experience managing crossfunctional clinical teams, including data management, statistician, site management and drug supply.
  • Strong program, project and time management skills; independently set direction and prioritize activities to drive execution.
  • Proficient in Microsoft Office Suite (Word, Excel, Access, Project, PowerPoint).
  • Excellent oral/written communication and interpersonal skills.
  • Strong research, analytical, criticalthinking, and problemsolving skills.
  • Ability to work in a fastpaced, deadlinedriven environment and to adapt to changing priority schedules.

Benefits:

  • Company computer
  • Eco vouchers
  • Flexitime
  • Hospitalization insurance
  • Retirement plan

Schedule:

  • Monday to Friday

Experience:

  • Administrative: 1 year (preferred)

Language:

  • Dutch (required)
  • English (required)

Work Location:
Hybrid remote in 3500 Hasselt
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