LOCATION: Freiburg, Germany (Remote)
This position reports to our Freiburg, Germany office (Heinrich-von-Stephan-Straße 5 | 79100 Freiburg Germany) and is fully remote with no expected travel.
Who We Are:TriNetX connects healthcare organizations and researchers across the globe so they can see what's happening in real patient populations-not guesses, not simulations.
Our aim is simple and ambitious: Provide a clear path to trustworthy answers, whether your goal is to create promising new therapies, publish groundbreaking research, or improve health outcomes.
We keep identifiable data where it belongs-inside more than 11,000+ clinical sites across 20+ countries-preserving security, provenance, and granularity. Our trusted partnerships with providers ensure high-fidelity data, and a properly governed linkage back to individual patients.
At TriNetX, we enable life sciences, healthcare, and academic institutions to strengthen human health-with data you can trace, evidence you can defend, and answers you can trust.
Who We Are Looking For:
TriNetX, LLC has an immediate need for a Student Worker Monitor to join our team. TriNetX was founded on the idea that incorporating real-world data results in better clinical trial design, improves the site selection and patient recruitment process and generates real-world evidence (RWE) to advance the collective understanding of human health. This position requires a well-rounded individual who has demonstrated the ability to deliver results in a high-growth, dynamic, and fast-paced environment. We are looking for a highly motivated team player who brings a strong work ethic and analytical skills.
What You Will Be Doing:
- 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
- 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
To learn more about us, please check out our website, blog, and Careers page - and be sure to follow us on LinkedIn.
Interested in joining our community?
TriNetX is an Equal Opportunity Employer. All persons are considered for employment without regard to their race, color, creed, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex or gender, marital status, sexual orientation, genetic information, gender identity, veteran status, or any other characteristic or status protected by applicable federal, state or local laws.
This Organization Participates in E-Verify
This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before.