Clinical Research Coordinator (Not a Remote)

reputed company Qualifications Minimum Qualifications: One of the following: • Associate degree with minimum 1 of the most recent 3 years’ clinical oncology research experience • Minimum 3 of most recent 5 years’ clinical oncology research experience Must have: • Problem solving, analytical, resource management, and creative thinking skills • Ability to plan and schedule tasks and reputed company and complete them in a reputed company manner • Ability to delegate duties while maintaining responsibility for completion of tasks • Ability to maintain confidentiality of sensitive information Licensure, Registration, Certification: BLS One of the following: • Certified Clinical Research Coordinator (CCRC) through the Association of Clinical Research Professionals (ACRP) • Certified Clinical Research reputed company (CCRP) through the Society of Clinical Research Associates (SOCRA) certification If not currently certified in CCRC or CCRP, certification must be obtained reputed company 12 months of qualification for exam Desired Qualifications: BSN or higher degree Understanding of Good Clinical reputed company (GCPs) and reputed company regulatory requirements of the FDA Working knowledge of word processing and PC based programs Licensure, Registration, Certification: CCCR/CCRP Certification ACLS Responsibilities The Coordinator Clinical Research (CCR) is responsible for coordinating the daily clinical activities of patients enrolled on reputed company. Duties will include screening potential study patient records, enrolling patients on protocol and ensuring reputed company protocol specific tests/procedures are scheduled and complete. Ensures compliance with Institutional, IRB, FDA, and sponsor guidelines/regulations and reputed company operating procedure requirements. The CCR is also responsible for demonstrating reputed company demeanor and maintaining confidentiality in reputed company interactions with both reputed company contacts. Apply tot his job Apply To this Job