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. We are currently looking for an experienced Clinical Research Associate (CRA) to support cell and gene therapy clinical trials at sites in Germany.
Please keep in mind that this role is a direct-hire at one of our clients a Big Pharma company.
Key Responsibilities
Manage site start-up initiation monitoring (remote and onsite) and close-out activities
Ensure protocol GCP and regulatory compliance at site level
Perform SDV/SDR CRF review and data quality oversight according to the monitoring plan
Support investigators and site staff through training and ongoing guidance
Drive site performance proactively identifying and resolving issues
Ensure timely reporting of SAEs and follow-up documentation
Maintain inspection readiness including ISF and essential documents
Ensure accurate and timely updates to CTMS and eTMF
Collaborate with data management patient safety and other stakeholders
Support audits and regulatory inspections as required
Qualifications
Bachelors degree in life sciences or a related field
Proven CRA experience in Cell & Gene Therapy (essential)
Strong knowledge of ICH-GCP and applicable local regulations
Solid understanding of clinical trial processes monitoring and data management
Experience with risk-based monitoring and remote monitoring approaches
Willingness to travel as required
Fluency in English and German
Must be based in Hamburg or Munich
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.
About this roleTFS 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 (F...
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. We are currently looking for an experienced Clinical Research Associate (CRA) to support cell and gene therapy clinical trials at sites in Germany.
Please keep in mind that this role is a direct-hire at one of our clients a Big Pharma company.
Key Responsibilities
Manage site start-up initiation monitoring (remote and onsite) and close-out activities
Ensure protocol GCP and regulatory compliance at site level
Perform SDV/SDR CRF review and data quality oversight according to the monitoring plan
Support investigators and site staff through training and ongoing guidance
Drive site performance proactively identifying and resolving issues
Ensure timely reporting of SAEs and follow-up documentation
Maintain inspection readiness including ISF and essential documents
Ensure accurate and timely updates to CTMS and eTMF
Collaborate with data management patient safety and other stakeholders
Support audits and regulatory inspections as required
Qualifications
Bachelors degree in life sciences or a related field
Proven CRA experience in Cell & Gene Therapy (essential)
Strong knowledge of ICH-GCP and applicable local regulations
Solid understanding of clinical trial processes monitoring and data management
Experience with risk-based monitoring and remote monitoring approaches
Willingness to travel as required
Fluency in English and German
Must be based in Hamburg or Munich
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.
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