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.
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