Clinical Trial Associate III

Clinical Trial Associate III page is loaded## Clinical Trial Associate IIIremote type: Remotelocations: United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R5797Premier Research is looking for a Clinical Trial Associate III to join our Functional Services Provider (FSP) team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.* We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.* Your ideas influence the way we work, and your voice matters here.* As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.Join us and build your future here.**This CTA role will be working for our FSP business, and we require immediate availability to start.****The role is offered as a fixed term contract with an anticipated end date of late November 2026.****What you\’ll be doing:*** Assisting with eTMF (electronic Trial Master File) filing and administration on all studies including more complex studies* Supporting the Clinical Research Associate (CRA) and site personnel with site level document collection.* Coordinating logistics and planning of meeting, events, and training* Primary lead to disseminate announcements and training materials related to clinical system updates and enhancements, as required Co-Leads and participates in project team meetings, prepares meeting minutes, and maintains action/decision logs* Creating, maintaining and providing quality checks for tracking tools and database repositories.* Performs Clinical Inspection Readiness and Quality Management System activities (e.g., deviations and CAPAs)* Tracking non-TMF documents and study status.* Reporting document collection and tracking issues.* Maintaining and leading CTA team in clinical inspection readiness and supporting regulatory inspections and/or audits as required.**What we\’re searching for:*** 5 years clinical research “CTA-like” work and **must** include hands on experience of audit preparation* Exposure at working with within a smaller company environment is **essential*** Experience with CROs and vendors* TMF experienced with workflows, document statuses, structure, compliance review* Wingspan and Veeva experience will be considered as advantageous* Study finance support activities* Support metric reporting and compliance oversight meeting management including minutes, agenda, action items, etc.* Premier Research is more than a company – it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems.* Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies.* As a Premier team member, you have the power to make an impact, regardless of job title and location.* Our dedication to biotech and specialty pharma is unlike any other.* We provide our staff with innovative technologies and continuous learning.### Join Our NetworkIntroduce yourself to our Talent Team and we will reach out if there is a role that aligns with your experience and interests.Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high – we will not stop until we reach our goals. And we care about each other, about our customer and partners, and, most importantly, about all the patients that we touch with our work.
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