SubjectWell
51 - 200 employees
Founded 2012
🏥 Healthcare
📦 Logistics
💼 Consulting
💰 $35M Series B - SubjectWell on 2022-10
Healthcare • Logistics • Consulting
SubjectWell is a patient-recruitment and site-enablement company that connects sponsors, CROs, clinical sites, and brand marketers with patients for clinical trials and commercial programs. Using the SubjectWell+ technology platform plus a Patient Network of over 15 million people, multilingual clinically trained Patient Companions, and an extensive partner network, the company provides recruitment, secondary screening, site support, retention services, translation, and global logistics to accelerate enrollment and reduce site burden across therapeutic areas and geographies.
Freelance Study Coordinator – Oncology, Clinical Trials
🕒 June 24
🗣️🇩🇪 German Required
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SubjectWell
51 - 200 employees
Founded 2012
🏥 Healthcare
📦 Logistics
💼 Consulting
💰 $35M Series B - SubjectWell on 2022-10
Healthcare • Logistics • Consulting
SubjectWell is a patient-recruitment and site-enablement company that connects sponsors, CROs, clinical sites, and brand marketers with patients for clinical trials and commercial programs. Using the SubjectWell+ technology platform plus a Patient Network of over 15 million people, multilingual clinically trained Patient Companions, and an extensive partner network, the company provides recruitment, secondary screening, site support, retention services, translation, and global logistics to accelerate enrollment and reduce site burden across therapeutic areas and geographies.
📋 Description
• 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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