Regional Clinical Trial Coordinator – 1-year fixed term

This is a fully remote position, open to applicants in Germany.

📋 Description

• Collaborate with Clinical Trial Managers and other regional trial personnel, including CRAs, on clinical trial initiatives.

• Assist with various trial-related responsibilities while managing multiple projects concurrently.

• Act as a specialist in document management and associated clinical trial processes.

• Oversee electronic clinical trial management systems and ensure databases are current.

• Utilize various systems to gather information regarding trial progress.

• Facilitate effective communication with both internal and external stakeholders concerning team administrative duties.

• Aid the regional trial team in identifying challenges, formulating solutions, and executing them.

⛳️ Requirements

• Minimum of a high school diploma.

• Ideally, at least one year of experience in a clinical trial setting as a project assistant or similar role, preferably within a CRO.

• Familiarity with ICH-GCP, the clinical trials documentation lifecycle, and Good Documentation Practice is advantageous.

• Highly developed administrative and organizational abilities.

• Capacity to work independently and juggle multiple tasks.

• Proficiency in English.

• Excellent verbal and written communication skills, along with strong interpersonal skills in a multicultural team environment.

• Proficient in MS Office applications (Excel, Word, PowerPoint, Outlook, etc.).

• Experience with Veeva systems is a plus.

🏝️ Benefits

• Flexible working time options: remote work and adaptable hours, based on department and role.

• Extra days off (“bridge-days”).

• Subsidized staff restaurant and cafeteria, offering vegetarian and vegan options.

• A variety of training and development opportunities.

• Health promotion initiatives focusing on both physical and mental well-being.

• Coverage for public transport ticket expenses.