Student Worker, Data Monitor

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

📋 Description

• Oversee and assess clinical research data for accuracy, completeness, plausibility, and consistency.

• Ensure adherence to study protocols and regulatory standards.

• Identify and promptly address any data discrepancies or issues.

• Validate the accuracy of all rules within the data capture system by inputting test data.

• Liaise with study sites and data managers to resolve data quality issues.

• Evaluate data management plans.

• Assist in creating and implementing data quality assurance procedures.

• Aid in the preparation of reports and presentations regarding data monitoring activities for both internal and external stakeholders.

• Coordinate resource planning and all monitoring activities in collaboration with the head of project management.

• Manage site administration tasks and maintain accurate records.

• Collaborate within interdisciplinary teams, including but not limited to project management, data management, data operations, medical advisors, and pharmacovigilance.

• Help train monitors in conjunction with PM, DM, and Medical Advisors.

• Assist in the setup and testing of electronic questionnaires and documentation forms.

• Contribute to pharmacovigilance-related activities.

• Manage participants in medical data collection surveys.

• Support adherence to quality standards, project specifications, and compliance regulations throughout the project lifecycle.

• Assist in process optimization and updating of SOPs and work instructions.

⛳️ Requirements

• Completed training in the healthcare field; additional certification as a monitor or similar is preferred.

• Experience in clinical research, data management, or a related area.

• Strong attention to detail along with excellent analytical skills.

• Outstanding communication and interpersonal abilities.

• Capability to work autonomously and collaboratively within a team.

• Familiarity with electronic data capture systems.

• Proficient knowledge of MS Office, particularly Word and Excel.

• Understanding of regulatory guidelines and Good Clinical Practice (GCP) standards.

• Team-oriented, adaptable, with exceptional communication skills.

• Proficient in both written and spoken German and English.

🏝️ Benefits

• Health insurance.

• Opportunities for professional development.

• Flexible working hours.