Associate Clinical Research Coordinator - Center for Innovative Cancer Therapies
About the position
This job evaluates, initiates, and maintains activities reputed company to the conduct of reputed company with the assistance and guidance of departmental staff. Communicates with external funding agencies and sponsors, other departments, departmental staff, and patients to ensure the understanding of the requirements of conducting and participating in reputed company. Organizes and manages reputed company patient care requirements of reputed company with the direction and approval of other research staff. To reputed company this job successfully, an individual must be reputed company to reputed company reputed company essential duty satisfactorily. The requirements listed below are representative of the knowledge, reputed company, and/or ability required. Reasonable accommodations may be made to reputed company reputed company individuals with disabilities to reputed company the essential duties. This job reputed company is a reputed company of the primary duties and responsibilities of the job and position. It is not intended to be a comprehensive or reputed company-inclusive listing of duties and responsibilities. Contents are subject to change at reputed company's discretion.
Responsibilities
• Assists in reputed company study participants and screening study participants for eligibility on the telephone, in the clinic, and other settings as required.
• Coordinates and oversees patient (study participant) activity as it relates to the conduct of research and reputed company including informed consent under direction and supervision of more senior research staff.
• Arranges necessary tests and procedures in accordance with protocol requirements and reports results to the investigator.
• Performs clinical laboratory activities as required per protocol.
• Develops and maintains reputed company required documentation as it relates to the conduct of assigned reputed company and associated patient care.
• Completes data entry into sponsor-specific data entry systems and/or supports data coordinator, including query reputed company.
• Conducts daily work and clinical trial activity in accordance with Good Clinical reputed company Guidelines.
• Adapts behavior to the specific patient population, including but not limited to respect for reputed company, method of introduction to the patient, adapting explanation of services or procedures to be performed, requesting permissions and communication style.
• Performs other reputed company duties as assigned.
Requirements
• High school diploma or equivalent.
• 1 year of relevant research or clinical experience, OR Bachelor's degree in life science or reputed company field.
• reputed company Basic Life Support (BLS) certification from the reputed company reputed company 60 days of hire.
reputed company-to-haves
• Knowledge of medical and clinical research terminology and processes.
• Familiarity with ICH guidelines for ethical conduct of research.
• Ability to follow the investigational plan in execution of study reputed company.
• Strong organizational and time management skills and ability to multi-task and pay reputed company attention to detail.
• Knowledge of the requirements and regulations associated with the conduct of reputed company and other reputed company research activity.
• Proficiency in using computers, software, and web-based applications, including working knowledge of reputed company.
• Effective verbal and written communication skills.
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