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SubjectWell

The global patient recruitment platform

Freelance Study Coordinator – Oncology, Clinical Trials

Location

Worldwide

Posted

22 hours ago

Salary

0

Seniority

Senior

Postgraduate Degree3 yrs expGermanEnglish

Job Description

Freelance Study Coordinator – Oncology, Clinical Trials

SubjectWell

• 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.

Job 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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