Sr. Clinical Project Manager

il y a 1 semaine

Brussels, Belgique BeCRO Temps plein

Position Summary

The Sr. Clinical Project Manager collaborates with the business development team and engages with clients to generate new business opportunities. The Sr. Clinical Project Manager is also 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
- Collaborate with the business development team and engage with clients to generate new business opportunities for Clinical Operations.
- 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, maintains 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, 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.

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