The role of Clinical Trials Assistant I offers a chance to work with clinical research projects in various therapeutic areas.
Responsibilities will include data management, creation of study-related documents, and correspondence with internal departments, research sites, and clients.
We are seeking a qualified professional to join our team in Frankfurt, Germany. Occasional home-office is possible after onboarding.
Key Responsibilities:
* Ensure the complete and accurate delivery of Trial Master Files.
* Support Clinical Research Associates (CRAs) and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.
* Assist the clinical team with preparing, handling, distributing, filing, and archiving clinical documentation and reports.
* Support CRAs and RSU teams with preparation, handling, and distribution of Clinical Trial Supplies and maintenance of tracking information.
* Track and manage Case Report Forms (CRFs), queries, and clinical data flow.
* Serve as a central contact for the clinical team for designated project communications, correspondence, and associated documentation.
* May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
Required Skills and Qualifications:
* Bachelor's or higher-level degree in life science or an apprenticeship in the medical field/office management including experience in the pharmaceutical field.
* Fluent German language skills at C1 level and good command of English.
* Computer skills including working knowledge of Microsoft Word, Excel, and PowerPoint.
* Effective communication, organizational, and planning skills.
* Ability to work independently and effectively prioritize tasks while working on multiple projects.
* Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Please apply with your CV, motivation letter, and certificates and reference letters.