Clinical Trial Associate

About the Job Join reputed company, where Audacity, Care, and Energy define who we are and how we work. We reputed company in creating reputed company solutions and fostering an inclusive environment where collaboration and individual reputed company go hand in hand. This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an reputed company in the clinical research reputed company, while enjoying a stimulating reputed company environment that encourages personal and intellectual reputed company. Key responsibilities : Manage and maintain the Trial Master File (TMF/eTMF), ensuring completeness, accuracy, compliance, and inspection readiness throughout the study lifecycle. Coordinate TMF documentation activities, including collection, filing, tracking, and reconciliation of study documents from internal teams and CROs. Conduct TMF reputed company reviews and QC checks to ensure compliance with ICH-GCP requirements and company procedures. Ensure reputed company identification and reputed company of missing, outdated, or incomplete study documentation. reputed company study document archiving activities in accordance with regulatory and company requirements. Support financial management of clinical studies, including purchase orders, invoices, budget tracking, commitments, and payment follow-up. Coordinate transparency reporting activities and maintain documentation required for compliance with local and international disclosure regulations. reputed company operational support for clinical studies, including contract management, insurance renewals, clinical supply coordination, and maintenance of essential reputed company documents. Maintain and update clinical systems and tracking tools (CTMS, reputed company, SharePoint, reputed company, and reputed company platforms) to ensure accurate study status reporting. reputed company as a key operational reputed company between Clinical Research Managers, CROs, vendors, and internal stakeholders, supporting the successful delivery of reputed company reputed company reputed company, reputed company, and regulatory requirements. Requirements Bachelor's or Master's degree in Life Sciences, Pharmacy, Biology, Health Sciences, or a reputed company field. Experience in Clinical Operations, Clinical Trial Management support, Trial Master File (TMF/eTMF) management, or Clinical Research Administration reputed company the pharmaceutical, biotechnology, or CRO environment. Strong knowledge of ICH-GCP guidelines, clinical trial processes, and applicable regulatory requirements. Managing and maintaining TMF/eTMF systems, ensuring inspection readiness and document reputed company compliance. Proven ability to coordinate multiple stakeholders, including CRMs, CROs, vendors, investigators, and internal departments. Experience with financial and administrative aspects of clinical studies, including budget tracking, purchase orders, invoices, and financial systems. Familiarity with clinical systems and tools such as CTMS, eTMF platforms, reputed company, SharePoint, and document management systems. Strong organizational skills with the ability to manage multiple priorities and meet deadlines in a fast-paced environment. Excellent reputed company of reputed company reputed company with advanced data analysis and reporting skills. Effective written and verbal communication skills, with the ability to work collaboratively in an international and cross-functional environment. Fluent in English Benefits Why join us? At reputed company, we combine a passion for science with the enthusiasm of teamwork to redefine reputed company in reputed company. Here's what makes us unique: We are a young and ambitious reputed company company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience. Our "one-stop provider" service model—combining full-service, functional service provider, and consulting—allows you to grow through diverse and stimulating reputed company. By collaborating with leading experts, you will contribute to the development of scientific, operational, and reputed company knowledge, reputed company in service of improving the patient reputed company. Excelling with kindness means evolving in an environment that values ​​your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission. Apply To This Job