Lead global clinical studies in a biopharma company aimed at improving public health. Collaborate with cross-functional teams to ensure quality and compliance in study delivery.
Responsibilities
Lead the planning and delivery of a global clinical study.
Act as the point of accountability for study delivery, quality and risk management from setup to archive.
Define and drive the study delivery plan, including feasibility, timelines, data capture strategy and quality controls.
Lead and coordinate cross-functional and vendor teams to ensure on-time and compliant study execution.
Identify, assess and manage study risks; escalate issues and implement mitigation plans.
Contribute to protocol development and regulatory submissions.
Requirements
Bachelor’s degree in life sciences, pharmacy, nursing, medicine or a related discipline.
Minimum 5 years’ experience in clinical development, clinical operations or study management in industry or CRO.
Proven experience leading global study setup and delivery across multiple countries.
Solid knowledge of Good Clinical Practice and clinical trial regulations.
Experience managing outsourced vendors and external partners for study execution.
Fluent English, with strong written and verbal communication skills.
Benefits
Private healthcare
Additional paid days off
Life insurance
Private pension plan
Fully paid parental leave & care of family member leave
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