Lead Clinical Research Associate - Freelance

TFS HealthScience; Remote; EUR 60.000 - 80.000; Teilzeit

Zusammenfassung

A leading global Contract Research Organization is seeking a Freelance Lead Clinical Research Associate to oversee site-level clinical trial activities in Germany. The role demands a university degree in Life Sciences or related field, with 6-8 years of CRA experience. Responsibilities include leading feasibility activities, managing regulatory submissions, and ensuring compliance with ICH-GCP and local regulations. This position offers flexible freelance engagement and competitive compensation.

Leistungen

Competitive compensation

Flexible freelance engagement

Collaborative work environment

Qualifikationen

• Minimum 6-8 years of CRA experience, including Lead CRA or Senior CRA responsibilities.
• Strong knowledge of ICH-GCP, EU and German regulatory requirements.
• Proven experience with site contracting, budgeting, and regulatory submissions.

Aufgaben

• Lead local feasibility activities, including site identification and evaluation.
• Oversee CDA management, site contracting, and site budget negotiations.
• Manage regulatory submissions, amendments, and local authority interactions.
• Lead and perform site initiation, monitoring, and close-out activities.

Kenntnisse

CRA experience

Site contracting

Regulatory knowledge

Stakeholder management

Fluency in German

Fluency in English

Ausbildung

University degree in Life Sciences, Pharmacy, Nursing, 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 Provider (FSP) solutions.

The Freelance Lead Clinical Research Associate (Lead CRA) is responsible for leading and overseeing site-level clinical trial activities in Germany, ensuring studies are conducted in compliance with ICH-GCP, local regulations, sponsor SOPs, and project timelines.

As part of our SRS / FSP team, you will be dedicated to one sponsor, a global pharmaceutical company recognized as an industry leader in innovative drug development across multiple therapeutic areas.

Please keep in mind that this is a freelance opportunity for approximately 0.8-1.0 FTE.

Key Responsibilities

• Lead local feasibility activities, including site identification and evaluation in Germany
• Oversee CDA management, site contracting, and site budget negotiations in collaboration with sponsors and vendors
• Manage regulatory submissions, amendments, and local authority / ethics interactions
• Lead and perform site initiation, monitoring, and close-out activities, ensuring high-quality trial execution
• Provide proactive site management and communication, acting as the primary escalation point for site-related issues
• Ensure accurate local documentation management, including TMF / ISF completeness and inspection readiness

Qualifications

• University degree in Life Sciences, Pharmacy, Nursing, or a related field
• Minimum 6–8 years of CRA experience, including Lead CRA or Senior CRA responsibilities
• Strong knowledge of ICH-GCP, EU and German regulatory requirements
• Proven experience with site contracting, budgeting, and regulatory submissions
• Excellent communication and stakeholder management skills
• Fluency in German and English (written and spoken)
• Experience working with oncology, especially breast cancer required.
• Experience working with RWE, non-interventional studies is required.

What We Offer

We provide a competitive compensation structure, flexible freelance engagement, and the opportunity to work with a leading global sponsor on impactful clinical trials. You will be part of a collaborative and professional environment that values expertise, quality, and long-term partnerships—while maintaining the flexibility of freelance work.

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 making a difference for patients worldwide.