SubjectWell/Clariness is a leading provider of solutions for clinical trial management, dedicated to accelerating patient enrollment in oncology trials. As a Freelance Study Coordinator, you will join our dedicated team and contribute to the swift completion of trials to ensure that innovative treatments reach patients sooner.
Our mission is to help patients access life-changing medications through meaningful communication and support. You will support cancer patients in understanding and participating in clinical trials, ensuring they feel informed and supported throughout the process. Your role will be to conduct unscripted, empathetic conversations with patients about clinical trial options, explaining the purpose, process, and risks of the trials using language that patients can understand.
Key responsibilities include:
- Clearly explaining the purpose, process, and risks of clinical trials to patients using language they can understand.
- Introducing relevant studies based on general criteria, such as cancer type and treatment setting.
- Encouraging informed discussions between patients and their treating physicians.
- Coordinating initial outreach between physicians and research sites when a trial may be suitable.
- Maintaining ethical standards in communication and respecting patient autonomy at all times.
- Ensuring proper documentation and confidentiality across all patient interactions.
Requirements:
- Medical degree (MD or equivalent) – required.
- At least 3 years of experience in oncology, clinical trials, or patient education.
- Prior involvement in oncology trials or patient recruitment is a strong plus.
- Familiarity with clinical trial workflows, patient navigation, or healthcare communication.
- Fluent German – required.
- Professional English – required.
- Professional Spanish - nice to have.
- Empathetic, professional communicator comfortable with sensitive topics.
- Strong organizational and coordination skills.
- Able to explain medical concepts without providing clinical advice.
- Respectful of ethical boundaries and patient autonomy.
- Competitive project-based compensation.
- Exposure to innovative oncology clinical trials.
- Meaningful work supporting cancer patients and clinical research.
- Exposure to innovative oncology clinical trials.
We are dedicated to fostering an inclusive and respectful working environment and welcome applications from professionals of diverse backgrounds.
Interested in contributing to meaningful medical research and helping patients access life-changing treatments? Apply now to join our team.
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