Global Clinical Trial Lead — Remote

Parexel International

Germany (OH)

On-site

USD 81,000 - 115,000

Full time

14 days+
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Job summary

Parexel is recruiting a Global Trial Leader in Germany for a phase 3 trial in Oncology or Inflammation. You will lead the trial team, oversee planning, execution, and delivery, and ensure milestones are met with input to sponsor pipelines.

The role focuses on GCP compliance, risk mitigation, and cross-functional collaboration. You will liaise with the Clinical Delivery team and CTM, manage budgets, and help prepare core trial documents while maintaining timely, complete documentation for all

Qualifications

  • Minimum of 5 years of relevant clinical trial management experience.
  • Strong clinical trial project management experience.
  • In-depth understanding of project management with emphasis on teamwork.
  • Experience in Oncology and/or Inflammation.
  • Extensive experience in international clinical trial project management.

Responsibilities

  • Provide leadership and direction to the trial team and be accountable for overall trial delivery.
  • Manage planning, implementation and tracking of clinical trial processes and risk mitigation.
  • Coordinate with CTM and other functions to ensure timely data delivery and regulatory compliance.
  • Oversee outsourcing and vendor management including Central Lab as applicable.
  • Support amendments, training, and responses to authorities as needed.

Skills

Clinical trial management
Project management
Team leadership
GCP awareness

Education

Masters degree (preferred)

Job description

Parexel is recruiting a Global Trial Leader in Germany for a phase 3 trial in Oncology or Inflammation. You will lead the trial team, oversee planning, execution, and delivery, and ensure milestones are met with input to sponsor pipelines.

The role focuses on GCP compliance, risk mitigation, and cross-functional collaboration. You will liaise with the Clinical Delivery team and CTM, manage budgets, and help prepare core trial documents while maintaining timely, complete documentation for all

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