Director Project Management - Freelance

TFS HealthScience; München; Vor Ort; EUR 125.000 - 150.000; Teilzeit

Zusammenfassung

A global mid-size Contract Research Organization is seeking a Director, Project Management to lead oncology projects with a strong focus on breast cancer studies. This part-time freelance position requires 10+ years of clinical project management experience and a university degree in a relevant field. The role includes strategic oversight and ensuring robust operational planning and quality governance across multiple regions. The organization values collaboration and innovation, providing a competitive compensation package and opportunities for professional growth.

Leistungen

Competitive compensation package

Comprehensive benefits

Opportunity for personal and professional growth

Qualifikationen

• 10+ years of experience in clinical project management in a CRO or pharmaceutical environment.
• Experience in breast cancer studies within oncology clinical trials.
• Strong knowledge of EU regulatory requirements and observational study regulations.

Aufgaben

• Lead operational planning aligning with sponsor priorities and budget.
• Provide oversight on feasibility, site contracting, and regulatory submissions.
• Ensure quality governance and maintain inspection readiness.

Kenntnisse

Leadership in Oncology clinical trials

Stakeholder management

Communication skills

Knowledge of ICH-GCP

Ausbildung

University degree in Life Sciences, Pharmacy, Medicine

Master’s degree preferred

Jobbeschreibung

About this role

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions.

The Director, Project Management is responsible for providing strategic and operational leadership across complex oncology projects. This role ensures end-to-end delivery excellence, timeline ownership, risk mitigation, and high-quality execution across multiple countries.

As part of our SRS/FSP team, you will be dedicated to one sponsor, a global pharmaceutical company with a strong commitment to evidence generation across the product lifecycle.

Please keep in mind that this is a part-time freelance opportunity at approximately 0.3 FTE.

Key Responsibilities

• Lead annual and monthly operational planning, ensuring alignment with sponsor priorities, resourcing, and budget expectations
• Provide strategic oversight of feasibility, site contracting, regulatory submissions, and amendments across multiple countries
• Drive cross-country harmonisation of study documents, processes, and operational standards
• Ensure robust TMF oversight and quality governance, maintaining inspection readiness at all times
• Track, analyse, and report KPIs to senior stakeholders
• Prepare, lead, and follow up on governance and steering committee meetings, ensuring clear decision-making and action tracking

Qualifications

• University degree in Life Sciences, Pharmacy, Medicine, or a related field; Master’s degree preferred
• Extensive experience (10+ years) in clinical project management within a CRO or pharmaceutical environment
• Demonstrated leadership experience in Oncology clinical trials, with a strong focus on breast cancer studies
• Proven expertise in Real World Evidence (RWE), Non-Interventional Studies
• Strong knowledge of ICH-GCP, EU regulatory requirements, and observational study regulations
• Excellent stakeholder management, communication, and leadership skills across cross-functional and cross-country teams

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for continued personal and professional growth in a strategic leadership role. You will work in a highly collaborative environment with exposure to innovative oncology programs and senior decision-makers, while having a direct impact on study delivery and patient outcomes.

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working toward a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability guide our decisions at every level. By aligning on these values, we foster a culture of collaboration, innovation, and excellence. Together, we make a difference.