FULL-TIME
Posted Sep 25, 2026
Job Description
Company Description Vincere Cancer Center is a patient-focused oncology practice dedicated to delivering high-quality, evidence-based cancer care in a supportive environment. The center emphasizes personalized treatment plans, multidisciplinary collaboration, and access to advanced therapies and clinical research. Team members work closely with patients and families to provide education, coordination of care, and compassionate support throughout the treatment journey. Vincere Cancer Center values innovation, integrity, and continuous improvement in both clinical practice and research. The organization encourages professional development and teamwork to improve outcomes and experiences for individuals affected by cancer.
Role Description: The Clinical Research Coordinator is a full-time, on-site role based in Scottsdale AZ. This position is responsible for coordinating and managing day-to-day activities for oncology clinical trials, including patient screening, enrollment, and follow-up. The coordinator will organize study visits, collect and document data, maintain regulatory and study files, and ensure adherence to protocols, regulatory requirements, and ethical standards. Daily responsibilities include communicating with patients and families about study procedures, collaborating with physicians and clinical staff, preparing study-related materials, and reporting adverse events and outcomes as required. The role also involves regular interaction with sponsors, monitors, and institutional stakeholders to support study start-up, ongoing monitoring, and close-out activities.
Qualifications
• Candidates should possess strong knowledge of informed consent processes, including explaining study aims, risks, and benefits, and documenting consent accurately.
• Candidates should possess skills in understanding and implementing study protocols, including scheduling visits, performing required assessments, and ensuring protocol compliance.
• Candidates should possess experience in research and clinical research activities, such as data collection, source documentation, and maintaining regulatory binders.
• Candidates should possess clinical research experience specific to oncology or related fields, with familiarity in managing clinical trials and coordinating with multidisciplinary teams.
• Candidates should possess skills related to clinical trials operations, including communication with sponsors and monitors, reporting adverse events, and preparing for audits or inspections.
• Associate’s or bachelor’s degree in a health-related or scientific field preferred; equivalent experience in clinical research considered.
• Certification as a Clinical Research Coordinator (e.g., ACRP, SOCRA) is beneficial but not required.
• Strong organizational, time-management, and documentation skills, with attention to detail and the ability to manage multiple studies concurrently.
• Effective written and verbal communication skills, with the ability to interact professionally and empathetically with patients, families, and healthcare professionals.
• Working knowledge of Good Clinical Practice (GCP), FDA regulations, and ethical standards related to human subjects research.
Role Description: The Clinical Research Coordinator is a full-time, on-site role based in Scottsdale AZ. This position is responsible for coordinating and managing day-to-day activities for oncology clinical trials, including patient screening, enrollment, and follow-up. The coordinator will organize study visits, collect and document data, maintain regulatory and study files, and ensure adherence to protocols, regulatory requirements, and ethical standards. Daily responsibilities include communicating with patients and families about study procedures, collaborating with physicians and clinical staff, preparing study-related materials, and reporting adverse events and outcomes as required. The role also involves regular interaction with sponsors, monitors, and institutional stakeholders to support study start-up, ongoing monitoring, and close-out activities.
Qualifications
• Candidates should possess strong knowledge of informed consent processes, including explaining study aims, risks, and benefits, and documenting consent accurately.
• Candidates should possess skills in understanding and implementing study protocols, including scheduling visits, performing required assessments, and ensuring protocol compliance.
• Candidates should possess experience in research and clinical research activities, such as data collection, source documentation, and maintaining regulatory binders.
• Candidates should possess clinical research experience specific to oncology or related fields, with familiarity in managing clinical trials and coordinating with multidisciplinary teams.
• Candidates should possess skills related to clinical trials operations, including communication with sponsors and monitors, reporting adverse events, and preparing for audits or inspections.
• Associate’s or bachelor’s degree in a health-related or scientific field preferred; equivalent experience in clinical research considered.
• Certification as a Clinical Research Coordinator (e.g., ACRP, SOCRA) is beneficial but not required.
• Strong organizational, time-management, and documentation skills, with attention to detail and the ability to manage multiple studies concurrently.
• Effective written and verbal communication skills, with the ability to interact professionally and empathetically with patients, families, and healthcare professionals.
• Working knowledge of Good Clinical Practice (GCP), FDA regulations, and ethical standards related to human subjects research.
Additional Details
- City
- Queen Creek
- State
- Arizona
- Country
- US
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