About this role
TFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service Provider solutions.
The Clinical Trial Associate (CTA) 0.5 FTE supports clinical study teams by coordinating operational activities and ensuring accurate setup maintenance and closure of the Study Master File in compliance with GCP SOPs and regulatory requirements.
As part of our SRS team you will work in a dedicated assignment environment collaborating closely with CRAs Project Managers and other study team members to support the successful execution of clinical trials.
Key Responsibilities:
Initiate maintain and close the Study Master File in compliance with GCP
Set up and maintain study data in the Clinical Trial Management System
Act as point of contact for Study Master File related activities
Support regulatory submissions amendments and related documentation
Coordinate meetings prepare minutes and support study communications
Assist with audits inspections and study close out activities
Qualifications
Bachelors degree preferred
Knowledge of GCP and ICH guidelines
Strong organizational and documentation skills
Good written and verbal communication skills
Ability to manage multiple tasks in a fast paced environment
What We Offer
We provide a competitive compensation package comprehensive benefits and opportunities for personal and professional growth in a collaborative and supportive environment. You will be part of a team that values quality flexibility and making a meaningful impact on patients lives.
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 we build solution driven teams working towards a healthier future. With over 800 professionals worldwide TFS delivers tailored clinical research services in more than 40 countries offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values Trust Quality Passion Flexibility and Sustainability guide our decisions and shape our culture. They help us attract and retain engaged professionals and foster a collaborative environment where together we make a difference.
About this roleTFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service Provider...
About this role
TFS HealthScience is a leading global mid size Contract Research Organization that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities resourcing and Functional Service Provider solutions.
The Clinical Trial Associate (CTA) 0.5 FTE supports clinical study teams by coordinating operational activities and ensuring accurate setup maintenance and closure of the Study Master File in compliance with GCP SOPs and regulatory requirements.
As part of our SRS team you will work in a dedicated assignment environment collaborating closely with CRAs Project Managers and other study team members to support the successful execution of clinical trials.
Key Responsibilities:
Initiate maintain and close the Study Master File in compliance with GCP
Set up and maintain study data in the Clinical Trial Management System
Act as point of contact for Study Master File related activities
Support regulatory submissions amendments and related documentation
Coordinate meetings prepare minutes and support study communications
Assist with audits inspections and study close out activities
Qualifications
Bachelors degree preferred
Knowledge of GCP and ICH guidelines
Strong organizational and documentation skills
Good written and verbal communication skills
Ability to manage multiple tasks in a fast paced environment
What We Offer
We provide a competitive compensation package comprehensive benefits and opportunities for personal and professional growth in a collaborative and supportive environment. You will be part of a team that values quality flexibility and making a meaningful impact on patients lives.
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 we build solution driven teams working towards a healthier future. With over 800 professionals worldwide TFS delivers tailored clinical research services in more than 40 countries offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology Neuroscience Oncology and Ophthalmology.
Our core values Trust Quality Passion Flexibility and Sustainability guide our decisions and shape our culture. They help us attract and retain engaged professionals and foster a collaborative environment where together we make a difference.
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