Project Director (Germany)

TN Germany; München; Remote; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

A leading company in clinical research is seeking a Project Director to oversee a portfolio of clinical studies. This home-based role requires extensive experience in project management, strong leadership skills, and knowledge of regulatory requirements. The ideal candidate will drive project success while maintaining client satisfaction and compliance with quality standards.

Qualifikationen

• Minimum 15 years industry experience, 5+ in a CRO.
• At least 10 years in clinical project management.

Aufgaben

• Oversee a portfolio of projects and Project Managers.
• Ensure studies comply with quality standards and regulations.
• Manage contracts and financial aspects.

Kenntnisse

Leadership

Project Management

Communication

GCP Knowledge

Ausbildung

BSc in a relevant field

Master’s degree

PMP Certification

PRINCE2 Certification

Jobbeschreibung

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Overview

The Project Director is responsible for overseeing the conduct of a program or portfolio of clinical studies or large global multicentered trials with substantial budgets. The portfolio may include studies for specific clients or a group within the same therapeutic area or indication across multiple clients. The Project Director manages Project Managers (PMs) handling projects of varying sizes and complexities, from single-service studies to large, multi-protocol, global projects. They contribute to proposal development and business growth activities at a project level, leveraging their therapeutic and project management expertise.

Ideal Candidate

• Wants to contribute to the growth of a specialized CRO
• Is a hands-on leader
• Seeks involvement in both program and line management

Responsibilities

• Oversee a portfolio of projects and the Project Managers responsible for operational execution
• Ensure all studies meet therapeutic or client-specific requirements
• Represent the company to clients, maintaining satisfaction and clear communication of deliverables
• Ensure studies comply with quality standards, SOPs, GCPs, regulatory requirements, and ICH guidelines
• Manage contracts and financial aspects, including budgets and expenses
• Track project progress using timelines and analysis tools
• Maintain in-depth therapeutic and client-specific knowledge for the portfolio
• Apply learning across studies and clients
• Lead contingency planning and risk mitigation strategies
• Potentially lead operational input for proposals and pricing strategies
• Drive performance improvements and operational efficiencies
• Provide line management and contribute to leadership in project management

Work Environment

At Indero, you will collaborate with talented colleagues in a culture of innovation, reliability, and responsiveness. We offer a stimulating environment with growth opportunities.

Location & Travel

This is a home-based position in Germany. Regular travel, including overnight and international trips, is required.

About Indero

Indero specializes in dermatology and rheumatology research. Founded in 2000 and based in Montreal, it has a reputation for high-quality research and services, expanding across North America and Europe.

Indero is committed to equitable treatment and provides accommodations during recruitment. Only applicants legally authorized to work in Germany will be considered.

Ideal Profile

Education:

• BSc in a relevant field; a Master’s is an asset
• PMP or PRINCE2 certification is an asset

Experience:

• Minimum 15 years industry experience, 5+ in a CRO
• At least 10 years in clinical project management, including managing all project phases and vendor relations
• Experience with multi-region, multinational phase III trials
• Leadership in mentoring and coaching project managers
• Business development experience
• Dermatology experience is advantageous

Knowledge & Skills:

• Strong knowledge of GCP, Health Canada, FDA regulations