Clinical Project Manager

il y a 1 semaine


Brussels, 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, critical-thinking, and problem-solving skills.
- Proven ability to motivate and manage cross functional project teams. A minimum of Two (2) years’ experience managing cross-functional 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, critical-thinking, and problem-solving skills.
- Ability to work in a fast-paced, deadline-driven 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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