Site Activation Lead, Clinical Trials & Start-up

Visa Hunt; Portugal; Presencial; EUR 65 000 - 90 000; Tempo integral

Resumo da oferta

Worldwide Clinical Trials is seeking a Site Activation Project Manager to oversee activation activities across assignments in the therapeutic area. You will coordinate with functional groups, manage timelines and budgets, and ensure compliant site activation deliverables in line with GCPs and SOPs.

The role requires strong leadership, cross-functional collaboration, and solid experience in CRO/pharma site activation, with fluent English and regulatory acumen.

Qualificações

• Bachelor’s degree in medical/biological/health sciences or nursing.
• Minimum 4 years CRO/pharma experience in Start-up/Project/Site Management.
• Fluent English (spoken and written).

Responsabilidades

• Serve as the primary point of communication for start-up and maintenance activities.
• Oversee site activation activities to meet critical path, budget and timelines.
• Ensure accurate tracking and analysis of site activation metrics and documents.
• Support feasibility and site identification activities as needed.
• Coordinate Site Qualification and Selection processes with team members.
• Communicate project status to Sponsor and project team.
• Develop risk mitigation plans for deliverables.
• Ensure budget line items include site activation activities.
• Maintain Change Notification Form tracking and execution.
• Contribute to SOP and process improvement initiatives.
• Possibly contribute to proposals and bids for site activation.

Conhecimentos

Leadership

Project management

Site activation

Regulatory knowledge

English proficiency

Formação académica

Bachelor’s degree in life sciences or nursing

4+ years CRO/pharma site start-up experience

Ferramentas

MS Office

Clinical trial systems

Descrição da oferta de emprego

Worldwide Clinical Trials is seeking a Site Activation Project Manager to oversee activation activities across assignments in the therapeutic area. You will coordinate with functional groups, manage timelines and budgets, and ensure compliant site activation deliverables in line with GCPs and SOPs.

The role requires strong leadership, cross-functional collaboration, and solid experience in CRO/pharma site activation, with fluent English and regulatory acumen.