Project Coordinator - Language Specialist

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Project Coordinator – Language Specialist German / French / Spanish / Japanese Join Us and Make an Impact at the Forefront of Clinical Research Innovation We have successfully supported the world’s top 50 pharmaceutical companies and more than 750 biotech organizations, spanning 2,700 clinical trials across 100+ countries over the last five years. We are looking for a Project Coordinator – Language Specialist who combines strong project coordination and organizational capabilities with proficiency in German, French, Spanish, or Japanese , in addition to English. This is an exciting opportunity to use your language skills in a global professional environment while supporting international clinical research projects and collaborating with teams and stakeholders across different countries. Language Requirement – A Key Part of This Role We are specifically looking for candidates who are proficient in at least one of the following languages: German | French | Spanish | Japanese In addition, candidates should possess strong English written and verbal communication skills. Candidates with recognized language qualifications or B2-level proficiency or above (or equivalent) are preferred. Your language capabilities will complement your project coordination responsibilities and help you communicate effectively while working within a diverse, global environment.

As a Project Coordinator – Language Specialist , you will provide administrative and technical support to global project teams, independently planning, organizing, and coordinating assigned responsibilities. You will support initial study setup and ongoing study maintenance, maintain systems and database repositories, complete data entry, prepare reports, and collect data for analysis and review. You will also contribute to audit readiness, risk management, process improvement initiatives, and effective communication across project teams. Depending on your experience and assignment, you may act as a key point of contact for the Project Lead (PL) or Clinical Team Manager (CTM) and provide coordination support to junior Project Support Coordinators. What You’ll Do Coordinate, oversee, and complete assigned clinical trial activities in accordance with the applicable task matrix. Support the initial study setup and ongoing maintenance of study-specific systems, tools, trackers, and documentation. Perform department, internal, country, and investigator file reviews as assigned, document findings, follow up on resolutions, and escalate issues when necessary. Ensure assigned activities are completed on time, within budget, and according to established quality standards. Support study-specific documentation and maintain key trackers, including study team lists, project-specific training requirements, system access management, and project-level activity plans. Provide support for clinical trial systems such as CTMS, Oracle Activate, and eTMF, including access requests, study-level document tracking, audit readiness, and follow-up on non-compliance. Coordinate and organize client and/or internal meetings, including scheduling, preparation and distribution of meeting minutes, and follow-up on action items where required. Export and reconcile study metrics reports and, where applicable, analyze information and identify potential issues. Maintain vendor trackers and regularly review information for accuracy and completeness. Coordinate the compilation of Investigator Site File (ISF) templates and pharmacy binders under the guidance of the Clinical Team Manager. Participate in Kick-Off and Project Launch meetings, take meeting notes when required, and support initial study setup. Identify potential project risks or issues in a timely manner and escalate them to the appropriate stakeholders. Contribute to functional and cross-functional initiatives focused on process improvements and