Clinical Project Lead Oncology Cell Therapy

TFS HealthScience; Hamburg; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A global healthcare research organization based in Hamburg is seeking a Clinical Project Lead to oversee and execute oncology clinical studies. In this full-time role, you will ensure that projects meet regulatory compliance, manage timelines and budgets, and serve as the main contact for local and global teams. The ideal candidate will possess a relevant university degree, strong experience in clinical trials, and fluency in both German and English to effectively communicate with stakeholders.

Leistungen

Competitive compensation package

Comprehensive benefits

Opportunity for personal and professional growth

Qualifikationen

• Minimum 3-5 years experience in clinical research with a solid background in study management.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Excellent organizational and communication skills with the ability to build effective relationships.

Aufgaben

• Lead and coordinate oncology clinical studies at a local level.
• Ensure compliance with regulatory requirements and sponsor/CRO SOPs.
• Manage study timelines, budgets, and quality deliverables.

Kenntnisse

Fluent in German

Fluent in English

Oncology studies expertise

Hospital Experience

Basic Life Support

Ausbildung

University degree in Life Sciences, Nursing, Pharmacy or related field

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 (FSP) solutions.

The Clinical Project Lead is responsible for the planning execution and oversight of clinical studies at the country level ensuring delivery of high-quality data within timelines budget and regulatory compliance.

As part of our SRS team you will be dedicated to one sponsor a global pharmaceutical / biotech company that is an industry leader in Oncology drug development .

Key Responsibilities

• Lead and coordinate the execution of one or more oncology clinical studies at a local / country level.
• Ensure compliance with ICH-GCP regulatory requirements and sponsor / CRO SOPs.
• Oversee site feasibility selection initiation monitoring and close-out activities.
• Act as the main point of contact for investigational sites local study teams and global counterparts.
• Manage study timelines budgets and quality deliverables at the country level
• Identify risks and implement mitigation strategies to ensure successful study delivery.

Qualifications

• University degree in Life Sciences Nursing Pharmacy or related field.
• Minimum 35 years experience in clinical research with solid background in study management.
• Proven expertise in Oncology studies within a CRO or pharmaceutical environment.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Excellent organizational and communication skills with ability to build effective relationships with investigators and stakeholders.
• Fluent in German and English (written and spoken).

What We Offer

We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. Youll be joining a team that values collaboration innovation and making a difference in the lives of patients

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 are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments resulting in high employee engagement and satisfaction. By aligning on these fundamental values we cultivate a unified force geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.

Key Skills

• Hospital Experience
• Acute Care
• Basic Life Support
• ICU Experience
• Infusion Experience
• Triage
• TFS
• Conflict Management
• Nursing
• Critical Care Experience
• Epic
• Medication Administration

Employment Type: Full Time

Experience: years

Vacancy: 1