Freelance Study Coordinator (Oncology / Clinical Trials)

Accelerate patient enrollment in clinical trials with SubjectWell/Clariness, helping patients gain access to life-changing medications. We support biopharmaceutical companies and CROs in completing clinical trials faster so innovative treatments can reach patients sooner. If you enjoy helping people and have strong communication skills, join our virtual team and contribute to meaningful medical research. We are currently seeking a Freelance Study Coordinator to support our team in handling unscripted patient calls related to oncology clinical trials. If you have a medical background, excellent communication skills, and experience in oncology or clinical research, this could be a great fit. Tasks About the role As an Onco-Companion – Patient Recruitment, you will serve as a key link between cancer patients, their treating physicians, and clinical trial sites. Your mission is to help patients feel informed and supported as they consider research participation. You will not assess medical eligibility, but rather support understanding, encourage dialogue with care teams, and help coordinate communication with study sites. As an Onco-Companion – Patient Recruitment, you will: • 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 Education: • Medical degree (MD or equivalent) – required. Experience: • At least 3 years of experience in oncolo