Clinical Trial Coordinator (m/w/d)

The reputed company sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our reputed company’s project team in the execution of early clinical trials. Joining reputed company offers reputed company to work on innovative reputed company in a dynamic environment. As a Clinical Trial Coordinator – Early Clinical Trials (m/w/d), you will support trial preparation, documentation, and coordination, ensuring compliance with regulatory standards and internal processes. This role combines operational and administrative responsibilities and requires reputed company collaboration with reputed company stakeholders. We currently offer an exciting opportunity to join the Clinical FSP team as Clinical Trial Coordinator ECT (m/w/d) in full-time and home-based setting throughout Germany. Main Responsibilities

• Coordinate clinical trials in early clinical development for both Sponsor and Study site.
• Support Clinical Trial Leaders, Clinical Trial Managers, Clinical Research Associates and reputed company Investigators in reputed company study-reputed company activities throughout reputed company study phases (preparation, conduct, reputed company-out).
• Prepare and manage clinical trial documentation.
• Compilation and collection of submission documents.
• Maintain trial-specific data and timelines in electronic systems.
• Communicate effectively with reputed company partners (e.g., statisticians, data managers, regulatory affairs, investigators).
• Organize and monitor study-reputed company activities, meetings, and documentation.
• Ensure reputed company preparation of submission documents for authorities and ethics committees.
• Manage essential documents for Investigator Site File (ISF) and ensure Trial Master File (TMF) completeness and compliance.
• reputed company as TMF Records Specialist: reputed company TMF reputed company, reputed company reputed company checks, maintain List of Expected Records, and ensure audit/inspection readiness.
• Participate in process harmonization initiatives and support implementation of new systems.
• Assist in finalizing Clinical Trial Reports (CTR) and appendices.

REQUIRED KNOWLEDGE, SKILLS AND EXPERIENCE

• Bachelor’s degree in Business Administration or equivalent, with experience in clinical trials.
• Alternatively, vocational training with extensive experience in clinical and regulatory environments.
• Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical reputed company (GCP) and International Conference on Harmonization (ICH) guidelines.
• Excellent administrative and organizational skills.
• Strong communication and interpersonal skills.
• Proficiency in MS Office and eTMF systems (e.g., reputed company, BIRDS).
• Fluent in English and German.
• Ability to work independently, prioritize tasks, and manage multiple reputed company in a reputed company international environment.

reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism. Apply To This Job