PR
Clinical Trial Associate III
full-time•Bulgaria
About this role
Premier 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.
What you'll do
- The Clinical Trial Associate III will assist with eTMF filing and administration, support Clinical Research Associates, and coordinate logistics for meetings and training. They will also maintain clinical inspection readiness and support regulatory inspections as required.
About Premier Research
Premier Research International LLC (Premier) is a global leader in clinical research and consulting services with expertise in driving an efficient and effective path to market for the life sciences industry.
Premier is built with the needs of biotech in mind, turning breakthrough science into life-changing drugs, devices, and diagnostics by addressing trial complexity, overcoming development hurdles, and demonstrating product value.
Leveraging deep therapeutic expertise, innovative technology, and product development operational proficiency—from preclinical planning to clinical trial execution and commercialization—our integrated approach offers personalized, end-to-end solutions to identify the pertinent data and insight necessary to make informed decisions earlier and deliver accelerated development timelines for a smarter, faster path to approval.
Through our commitment to partner boldly, deliver impact, and foster community, we’re driving change that advances research and improves lives while creating meaningful opportunity for patients, customers, and all Premier team members. Follow our page to learn more about our work—and explore career opportunities to be part of the transformation.
Ready to join Premier Research?
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Frequently Asked Questions
What does a Clinical Trial Associate III do at Premier Research?
As a Clinical Trial Associate III at Premier Research, you will: the Clinical Trial Associate III will assist with eTMF filing and administration, support Clinical Research Associates, and coordinate logistics for meetings and training. They will also maintain clinical inspection readiness and support regulatory inspections as required..
Is the Clinical Trial Associate III position at Premier Research remote?
The Clinical Trial Associate III position at Premier Research is based in Bulgaria. Contact the company through Clera for specific work arrangement details.
How do I apply for the Clinical Trial Associate III position at Premier Research?
You can apply for the Clinical Trial Associate III position at Premier Researchdirectly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process.