Student Worker, Data Monitor

Job not on LinkedIn

🔥 1 minute ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

X

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

📱 Media

👥 B2C

💰 $1G Undisclosed on 2025-04

Media • B2C

X is a social media platform and app operated by X Corp (formerly Twitter). It provides a real-time public conversation service where users can sign in (phone, Google, Apple, or email/username), follow news and trending posts, access developer tools, and use features such as the Grok AI assistant. The service supports mobile apps, advertising/business tools, and public-facing content policies and terms of service.

📋 Description

• Monitor and review clinical research data for accuracy, completeness, plausibility and consistency • Ensure compliance with study protocols and regulatory guidelines • Identify and resolve data discrepancies or issues in a timely manner • Verifying the accuracy of all rules within the data capture system by entering test data • Communicate with study sites and data managers to address data quality concerns • Review data management plans • Assist in the development and implementation of data quality assurance processes • Support in generating reports and presentations on data monitoring activities for internal and external stakeholders • Resource planning and co-ordination of all monitors in consultation with head of project management • Manage site administration activities and maintain records • Work in interdisciplinary teams with (but not limited to) project management, data management, data operations, medical advisor, pharmacovigilance • Support in training monitors (in conjunction with PM, DM and Medical Advisor) • Support in setting up and testing electronic questionnaires /documentation forms • Support in pharmacovigilance related activities • Management of participants in medical data collection surveys • Assisting adherence to quality standards, project requirements, and compliance regulations throughout the project lifecycle • Support in process optimization and revision of SOPs and work instructions • Support in tasks related to other project management related activities

🎯 Requirements

• Completed training in the healthcare sector; further certification as a monitor or similar is desirable • Experience working in clinical research, data management, or related field • Strong attention to detail and analytical skills • Excellent communication and interpersonal skills • Ability to work independently and as part of a team • Knowledge of electronic data capture systems • Very good knowledge of MS Office, especially in Word and Excel • Knowledge of regulatory guidelines and Good Clinical Practice (GCP) standards • You convince through very structured work and a high degree of initiative, as well as a solution-oriented approach • You easily maintain a comprehensive understanding of project progress and status, with the ability to identify any potential issues or roadblocks • Team spirit, flexibility and excellent communication required • Ability to work in a changing and agile environment with international collaborations • Very good written and spoken German and English skills • Experience in oncology is of advantage but not a pre-requisite • Language skills additional to German and English are beneficial but not essential

🏖️ Benefits

• TriNetX is an Equal Opportunity Employer • Participants in E-Verify