Global Clinical Study Lead: Shape Self-Care Innovation

Opella

Neuilly-sur-Seine

On-site

EUR 71,000 - 95,000

Full time

2 days ago
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Job summary

Opella is reinventing self-care through science-driven innovation. As a Global Clinical Study Lead, you will lead the planning, execution and delivery of global clinical and evidence generation studies that support our OTC, VMS and Rx-to-OTC switch portfolios.

You will work with cross-functional teams and external partners to ensure studies are delivered on time, within budget and in compliance with quality and regulatory standards, while contributing to the evolution of evidence generation in

Qualifications

  • 8+ years of clinical study management experience within Pharma, Consumer Healthcare and/or CRO environments.
  • Strong project management and vendor management experience.
  • Experience in Consumer Healthcare and/or Rx-to-OTC switch programs is a strong advantage.
  • Solid knowledge of ICH-GCP and international clinical research standards.

Responsibilities

  • Lead end-to-end delivery of global clinical and evidence generation studies.
  • Oversee study activities from planning through close-out and archiving.
  • Manage CROs and external partners, ensuring high-quality delivery and performance.
  • Ensure compliance with ICH-GCP, applicable regulations and internal SOPs.
  • Drive continuous improvement across the Clinical Evidence organization.

Skills

Clinical study management
Project management
Vendor management
Cross-functional collaboration
ICH-GCP knowledge

Education

Bachelor's degree in a scientific discipline

Job description

Opella is reinventing self-care through science-driven innovation. As a Global Clinical Study Lead, you will lead the planning, execution and delivery of global clinical and evidence generation studies that support our OTC, VMS and Rx-to-OTC switch portfolios.

You will work with cross-functional teams and external partners to ensure studies are delivered on time, within budget and in compliance with quality and regulatory standards, while contributing to the evolution of evidence generation in

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