Director, Clinical Portfolio Execution

TN Germany; Marburg; Hybrid; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

An innovative biotechnology leader is seeking a Director of Clinical Portfolio Execution to enhance clinical trial operations and drive process improvements. This exciting role offers the opportunity to establish standards for study operations, coordinate with global resources, and lead initiatives that foster best practices in clinical research. With a commitment to employee well-being and an inclusive work environment, this position is ideal for seasoned professionals looking to make a significant impact in the pharmaceutical industry. Join a forward-thinking company dedicated to saving and improving lives through advanced biotechnology solutions.

Leistungen

Comprehensive health benefits

Financial security programs

Well-being support

Inclusive work environment

Qualifikationen

• 12+ years of clinical research experience in the pharmaceutical industry.
• Strong knowledge of drug development and clinical trial processes.

Aufgaben

• Manage standards for study operations activities and clinical trial support.
• Lead process improvements and ensure compliance with industry best practices.

Kenntnisse

Clinical Research

Project Management

Drug Development

Regulatory Compliance

Biological Sample Management

Ausbildung

Bachelor’s degree in Science or Pharmacy

Jobbeschreibung

The provided job description has a good structure but can benefit from improved formatting and focus. Here's a refined version:

Job Description

CSL Behring, a global biotechnology leader dedicated to saving and improving lives, is seeking a Director of Clinical Portfolio Execution. This role can be based in King of Prussia, PA; Marburg, Germany; or Bern, Switzerland, and offers a hybrid work model. The position reports to the Senior Director of Clinical Portfolio Execution and manages multiple direct reports.

Responsibilities

1. Establish and manage standards and processes for main study operations activities, including clinical trial support and biological sample management.
2. Facilitate global resource planning for clinical portfolio execution, ensuring alignment with project priorities and effective communication of resource management strategies.
3. Implement process improvements based on lessons learned from study conduct, audits, and inspections, ensuring adherence to industry best practices and ICH GCP guidelines.
4. Lead capability building initiatives, including onboarding and harmonization of practices at the study level.
5. Coordinate with Functional Service Providers for study delivery, oversee vendor activities, and contribute to staff training on CSL expectations.
6. Manage quality practices, develop control documents, and support training related to Study Delivery roles.

Qualifications

• Bachelor’s degree in Science or Pharmacy.
• At least 12 years of relevant experience in clinical research or related fields within the pharmaceutical industry.
• Strong understanding of the drug development and clinical trial processes.
• Experience in study management, clinical operations, and biological sample management.
• Knowledge of ICH GCP, FDA GCP regulations, and EU clinical trial directives.

Additional Information

CSL offers comprehensive benefits from day one, supporting employees' health, financial security, and well-being. We are committed to fostering an inclusive environment where all employees can thrive.