Clinical Project Leader: Deliver Trials with Impact

IQVIA LLC; Amsterdam; On-site; EUR 70,000 - 100,000; Full time

Job summary

IQVIA LLC is seeking a Clinical Project Manager to lead delivery of local clinical studies, ensuring timelines, quality and cost targets are met. The role requires close collaboration with cross-functional teams and ongoing client coordination.

The ideal candidate will have 5+ years of clinical research experience and strong knowledge of ICH GCP, with fluency in Dutch and English and willingness to work from Haarlem offices two days per week.

Qualifications

• Bachelor's degree in life sciences or related field.
• Minimum 3+ years as Project Manager and 5+ years clinical research experience.
• Knowledge of ICH GCP and local regulations.
• Fluency in Dutch and English, both written and spoken.
• Strong problem solving, planning and communication skills.
• Experience with project financials and contract obligations.
• Willingness to work at Sponsor's office in Haarlem for at least 2 days per week.

Responsibilities

• Delivery and management of smaller, less complex local studies.
• Develop integrated study management plans with the core project team.
• Execute clinical studies per contract while optimizing speed, quality and cost.
• Set objectives and assess performance for the core project team.
• Collaborate with cross-functional groups to achieve milestones.
• Monitor progress and report to stakeholders; manage risks and issues.
• Maintain project quality and implement corrective actions as needed.
• May serve as primary contact with customers and manage vendor relations.

Skills

Project management

Fluent Dutch

Fluent English

Problem solving

Planning

Communication

MS Office

Cross-cultural awareness

Financials understanding

Education

Bachelor's Degree Life sciences or related

Tools

MS Office

Job description

IQVIA LLC is seeking a Clinical Project Manager to lead delivery of local clinical studies, ensuring timelines, quality and cost targets are met. The role requires close collaboration with cross-functional teams and ongoing client coordination.

The ideal candidate will have 5+ years of clinical research experience and strong knowledge of ICH GCP, with fluency in Dutch and English and willingness to work from Haarlem offices two days per week.