Director Project Management - Freelance

TFS HealthScience; Essen; Vor Ort; EUR 80.000 - 100.000; Teilzeit

Zusammenfassung

A global Contract Research Organization is seeking a part-time Director, Project Management to lead complex oncology projects. This role requires over 10 years of clinical project management experience, preferably in Oncology. You will ensure delivery excellence and oversee processes across multiple countries while collaborating with a pharmaceutical sponsor. The position offers a competitive compensation package and the opportunity to impact patient outcomes and innovative oncology programs.

Leistungen

Competitive compensation package

Comprehensive benefits

Personal and professional growth opportunities

Qualifikationen

• 10+ years of clinical project management experience.
• Demonstrated experience in Oncology clinical trials.
• Strong focus on breast cancer studies.

Aufgaben

• Lead operational planning and alignment with sponsor.
• Provide oversight for feasibility, site contracting, and submissions.
• Drive harmonisation of study documents across countries.
• Ensure quality governance and inspection readiness.

Kenntnisse

Leadership in clinical trials

Stakeholder management

Communication skills

Knowledge of ICH-GCP

Oncology expertise

Ausbildung

University degree in Life Sciences or related field

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) and 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 towards 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.