Senior Manager, GCP Compliance

Takeda Pharmaceutical Co.; Województwo mazowieckie; Presencial; PLN 267.000 - 368.000; Jornada completa

Descripción de la vacante

Takeda Pharmaceutical Co. in Warsaw, Poland, is seeking an experienced quality/compliance professional to manage significant GCP compliance activities across R&D.

You will provide subject-matter expertise to strengthen inspection readiness, quality-system execution, risk management, and continuous improvement. You will lead quality-event investigations, coordinate audits, and collaborate with Clinical Trial Delivery, Medical, and other functions to drive sustainable improvements.

Formación

• A bachelor’s degree or equivalent experience.
• At least six years in pharma/ CRO.
• Solid knowledge of clinical trial management and GCP.
• Regulatory requirements for trials and industry best practices.
• Advanced drug development and trial process knowledge.
• Experience with clinical development training and process tools.
• Strong planning, execution, problem-solving, and communication.
• Experience working with stakeholders across functions using digital tools.

Responsabilidades

• Manage quality-system activities including changes, deviations and investigations.
• Provide compliance guidance to study teams and stakeholders.
• Lead quality-event investigations and corrective actions.
• Coordinate audit and inspection readiness.
• Analyze compliance metrics and trends for governance forums.
• Lead defined projects with cross-functional partners.
• Support continuous improvement from audit insights.

Conocimientos

GCP compliance

Regulatory knowledge

Project management

Stakeholder management

Communication

Educación

Bachelor’s degree or equivalent

Herramientas

MS Office

Descripción del empleo

Job Description

About the Role

In this role, you will independently manage significant Good Clinical Practice compliance activities across Research and Development. You will provide subject-matter expertise to strengthen inspection readiness, quality-system execution, risk management, and continuous improvement. Working with cross-functional stakeholders, you will help identify, assess, eradicate? The original: ... Actually we omitted.

How You Will Contribute

• Manage assigned quality-system activities including standards, procedures, change controls, deviations, incident escalation, investigations, and corrective and preventive actions.
• Provide compliance expertise and practical guidance to study teams, process owners, and Research and Development stakeholders.
• Lead quality-event investigations and corrective actions by coordinating root-cause analysis, effectiveness checks, risk escalation, and timely follow-up.
• Coordinate audit and inspection readiness through preparation, document review, request management, stakeholder support, response development, and post-inspection remediation.
• Analyze compliance metrics and trends to identify risks, recommend mitigation actions, and prepare reports for governance forums and leadership.
• Lead defined projects and workstreams while partnering with Clinical Trial Delivery, Medical, Research and Development Quality, and other functions.
• Support continuous improvement by translating audit and inspection lessons into practical, sustainable improvements.

Qualifications

• A bachelor’s degree or equivalent experience.
• At least six years of experience in the pharmaceutical industry and/or a clinical research organization.
• Solid knowledge of clinical trial management and Good Clinical Practice compliance processes.
• Comprehensive knowledge of regulatory requirements governing clinical trials and relevant industry best practices.
• Advanced knowledge of drug development and clinical trial processes, including related standards and documents.
• Experience with clinical development training and process management methods and tools.
• Strong planning, execution, problem-solving, negotiation, collaboration, and communication skills.
• Experience working effectively with stakeholders and teams without direct reporting relationships, using digital tools, Microsoft Office, project management, and presentation software.

Salary range:

267,400.00 PLN - 367,730.00 PLN

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.

Locations

Warsaw, Poland

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time