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You will be updated with latest job alerts via emailAbout this role
TFS HealthScience is a leading global midsize 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 a Clinical Trial Associate (CTA) to join our SRS team dedicated to one sponsor a leading company in the pharmaceutical industry. In this role you will support the clinical study team with key documentation tasks and ensure efficient and compliant management of study documentation throughout the trial lifecycle.
Key Responsibilities
Manage essential clinical trial documentation and support study teams with ongoing document updates
Oversee the preparation collection tracking and archiving of documents in line with regulatory and sponsor requirements
Support regulatory and ethics submissions as part of the study startup and maintenance process
Work within systems such as the UCTR (Unified Clinical Trial Registry) to maintain documentation and status updates
Collaborate closely with clinical and regulatory colleagues to ensure documentation accuracy and compliance
Qualifications
Previous experience in clinical research or document management ideally as a CTA or study coordinator
Good understanding of regulatory submissions and documentation requirements in clinical trials
Experience using clinical systems such as UCTR or other eTMF platforms is a plus
Detailoriented with strong organizational and communication skills
Ability to work independently and in collaboration with crossfunctional teams
Fluent in Spanish and comfortable working in English
What We Offer
We provide a competitive compensation package comprehensive benefits and the opportunity for personal and professional growth in a rewarding environment. You will 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 fullservice global Contract Research Organization (CRO) we build solutiondriven 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 decisionmaking at all levels of the organization. They assist us in attracting and retaining valuable talent who share our values resulting in high employee engagement and satisfaction. By aligning on these fundamentals 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.
Full Time