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.
Please keep in mind that this is a Part-time approximately 0.5 FTE Freelance Opportunity.
Key Responsibilities:
Perform monitoring activities for bioequivalence clinical studies in accordance with ICH-GCP SOPs and applicable regulatory requirements
Ensure subject safety data integrity and protocol compliance at investigational sites
Review clinical trial documentation source data and CRFs/eCRFs
Support site qualification initiation routine monitoring and close-out visits as required
Collaborate closely with study teams investigators and vendors including bioanalytical partners
Contribute to inspection readiness and quality oversight activities
Qualifications:
Previous experience within bioequivalence studies as Clinical Research Associate
Background or exposure to bioanalysis is highly desirable
Prior working relationship with Quinta is considered an advantage
R3 standard training completed
Fluency in Czech (spoken and written) is required; good command of English
Ability to work part-time (approximately 0.5 FTE) as freelancer
Based in or near Prague and able to travel locally as needed
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.
Please keep in mind that this is a Part-time approximately 0.5 FTE Freelance Opportunity.
Key Responsibilities:
Perform monitoring activities for bioequivalence clinical studies in accordance with ICH-GCP SOPs and applicable regulatory requirements
Ensure subject safety data integrity and protocol compliance at investigational sites
Review clinical trial documentation source data and CRFs/eCRFs
Support site qualification initiation routine monitoring and close-out visits as required
Collaborate closely with study teams investigators and vendors including bioanalytical partners
Contribute to inspection readiness and quality oversight activities
Qualifications:
Previous experience within bioequivalence studies as Clinical Research Associate
Background or exposure to bioanalysis is highly desirable
Prior working relationship with Quinta is considered an advantage
R3 standard training completed
Fluency in Czech (spoken and written) is required; good command of English
Ability to work part-time (approximately 0.5 FTE) as freelancer
Based in or near Prague and able to travel locally as needed
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.
View more
View less