Freelance Study Coordinator – Oncology, Clinical Trials

This is a fully remote position, open to applicants anywhere in the world.

📋 Description

• Act as a crucial liaison between cancer patients, their healthcare providers, and clinical trial facilities.

• Engage in genuine, unscripted conversations with cancer patients regarding their clinical trial options.

• Articulate the objectives, procedures, and potential risks associated with clinical trials in a manner that is easily understandable for patients.

• Present pertinent studies based on broad criteria such as cancer type, treatment context, and geographical location.

• Promote informed dialogue between patients and their healthcare providers.

• Facilitate initial contact between healthcare providers and research sites when a trial appears appropriate.

• Uphold ethical communication standards and consistently respect patient autonomy.

• Ensure accurate documentation and confidentiality in all patient interactions.

⛳️ Requirements

• Medical degree (MD or equivalent) – mandatory.

• Minimum of 3 years of experience in oncology, clinical trials, or patient education.

• Previous experience in oncology trials or patient recruitment is highly advantageous.

• Knowledge of clinical trial processes, patient navigation, or healthcare communication is essential.

• Proficiency in German – required.

• Professional proficiency in English – required.

• Professional proficiency in Spanish - preferred.

🏝️ Benefits

• Opportunity for remote freelance work.

• Competitive compensation based on project work.

• Fulfilling role that supports cancer patients and contributes to clinical research.

• Access to cutting-edge oncology clinical trials.