آخر تحديث: أغسطس 17, 2026
المسؤوليات
As part of this dynamic Cancer Center CTO team, Clinical Research Coordinators will manage & oversee several oncology clinical trials, from study inception to termination.
Responsibilities for this position include but are not limited to: activation & maintenance of the oncology clinical trials protocols; acting as liaison between physicians, clinic staff, UIC IRB office, الرعاة, & regulatory agencies; educating physicians & clinic staff on impact of protocol modifications & adverse events; assisting physicians & clinic staff in identification, recruitment, and enrollment of patients for clinical trial protocols; تخطيط & coordinating strategies for increasing patient enrollment at University and affiliate sites, acting as liaison between patients, الأطباء, & sponsors in patients’ enrollment compliance to regulations, especially FDA & NCI, and sponsor guidelines; reviewing protocols to ensure compliance with laboratory & clinic procedures & ensuring that evaluations are met; & providing expertise on clinical components regarding physician, patient, & clinic staff compliance.
Requirements
Bachelor’s degree in nursing (with current IL licensure to practice) plus 2 years clinical research experience required; oncology clinical research experience a plus. Proficiency with information systems & knowledge of federal regulations & guidelines regarding clinical trials preferred; SoCRA certification (or equivalent) a plus, and required within 2 years of hire. Requires excellent written, شفوي & interpersonal communication skills, as well as a strong ability to organize, prioritize, & coordinate multiple activities to meet deadlines. Experience with electronic medical records is desirable. Must be proficient in MS Office, including MS Access.
مراجعة الحالة العلمية
هل ترغب في فهم ما إذا كانت البرامج السريرية الحالية, التطورات البحثية الأخيرة, أو قد تكون النهج الناشئة ذات الصلة بحالتك الفردية?
شارك سؤالك مع فريق البحث العلمي لدينا واستقبله المعلومات التي تركز على مجالات البحث الحالية التي قد تكون ذات الصلة بحالتك.
- مراجعة المعلومات التي تقدمها
- البحوث ذات الصلة ومعلومات البرنامج السريري
- استجابة واضحة تركز على حالتك
لا التزام. سيتم مراجعة سؤالك بسرية.
المعلومات التعليمية والبحثية فقط. هذه الخدمة لا تشكل نصيحة طبية, تشخبص, روشتة, أو شخصية توصية العلاج.
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