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 Study Coordinator role serves as the primary contact person for sponsors potential clients and external service providers as well as for patients participating in clinical trials.
As part of our SRS/FSP team you will be dedicated to one sponsor.
Please keep in mind that this is a short-term contract position. The amount of work expected is approximately 1 month of full-time engagement (or longer depending on candidates availability).
Key Responsibilities
- Act as the main contact for sponsors ethics committees and study monitors
- Coordinate study operations documentation and audits
- Manage patient recruitment scheduling and study communication
Qualifications
- Minimum of 2 years of relevant experience in clinical research or a healthcare-related environment
- Professional experience as a Study Nurse Study Coordinator or a completed university degree in a natural science field
- Strong knowledge of ICH-GCP Guidelines
- Dutch language (mandatory) both written and spoken
- Willingness to travel to the site in Nijmegen
- Experience with cardiovascular studies is a big plus
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 (...
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 Study Coordinator role serves as the primary contact person for sponsors potential clients and external service providers as well as for patients participating in clinical trials.
As part of our SRS/FSP team you will be dedicated to one sponsor.
Please keep in mind that this is a short-term contract position. The amount of work expected is approximately 1 month of full-time engagement (or longer depending on candidates availability).
Key Responsibilities
- Act as the main contact for sponsors ethics committees and study monitors
- Coordinate study operations documentation and audits
- Manage patient recruitment scheduling and study communication
Qualifications
- Minimum of 2 years of relevant experience in clinical research or a healthcare-related environment
- Professional experience as a Study Nurse Study Coordinator or a completed university degree in a natural science field
- Strong knowledge of ICH-GCP Guidelines
- Dutch language (mandatory) both written and spoken
- Willingness to travel to the site in Nijmegen
- Experience with cardiovascular studies is a big plus
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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