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Development Environment Specialist at Exposant 3 focusing on technology transformation and digital organization. Involves collaboration and implementation of development practices and tools.
About the role
- Freelance Study Coordinator responsible for patient recruitment in oncology clinical trials. Helps patients understand their clinical trial options and connects them with research opportunities.
Responsibilities
- Serve as a key link between cancer patients, their treating physicians, and clinical trial sites.
- Conduct unscripted, empathetic conversations with cancer patients about clinical trial options.
- Clearly explain the purpose, process, and risks of clinical trials using language that patients can understand.
- Introduce relevant studies based on general criteria (e.g., cancer type, treatment setting, location).
- Encourage informed discussions between patients and their treating physicians.
- Coordinate initial outreach between physicians and research sites when a trial may be suitable.
- Maintain ethical standards in communication and respect patient autonomy at all times.
- Ensure 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.
Benefits
- Remote freelance opportunity.
- Competitive project-based compensation.
- Meaningful work supporting cancer patients and clinical research.
- Exposure to innovative oncology clinical trials.
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