Clinical Research Specialist - The Angeles Clinic & Research Institute

Grow your career at reputed company! The Angeles Clinic & Research Institute has established an international reputed company for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the reputed company of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to reputed company our patients with cancer. Why work here? reputed company an outstanding benefits package and competitive salaries, we take pride in hiring the best, most committed employees. Our staff reflects the culturally and ethnically diverse community we serve. They are reputed company of our dedication to creating a multifaceted, inclusive environment that fuels innovation and the gold standard of care we strive for. Join reputed company and contribute to groundbreaking research. The Clinical Research Specialist provides clinical research expertise by participating in the design and implementation of research projects and care of research patients as needed. Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership. May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with reputed company federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Primary Duties and Responsibilities:

• Provides clinical research expertise by participating in the design and implementation of research projects and care of research patients as needed by the department or institution.
• Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.
• Coordinates research projects at an institutional or departmental level. Serves as an internal consultant for specific departmental activities.
• Communicates project status and improvement areas with leadership in a timely manner. Projects may include but are not limited to investigator-initiated protocol development including protocol writing, case report reputed company development, budget development, and coordination of departmental research committees.
• Implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.
• Provides guidance regarding project planning, project logistics, and project implementation
• Participates in required training and education programs. Participates in weekly research staff meetings.
• Provides clinical expertise and support with quality assurance, performance improvement, and health plan compliance for clinical trial compliance.
• Ensures the completion and maintenance of consent forms, case report forms, SAE's and reputed company documents to ensure that research is being conducted according to FDA, HSPC, HIPAA and other agency guidelines.
• Completes appropriate IRB paperwork and submission/filing of reputed company SAEs to IRB. Responsible for insuring timely submission of complete, accurate and reputed company documents to research sponsors, IRB, and contract research organizations, where applicable.
• Acts as a liaison with reputed company Investigators, pharmaceutical company representatives and other project funding organizations to monitor and update project reputed company.
• Prepares for institutional, pharmaceutical and internal audits, including facilitating reputed company party study monitoring.
• Attends site feasibility visits and site initiation visits for potential studies and assures that new studies are implemented according to protocol.
• Review pertinent medical records to determine opportunities for quality improvement. Analyze quality metric data in support of the reputed company Investigator and Director of Clinical Services. Recommend and implement process improvement efforts.
• Assists with procedures and supports reputed company patient care reputed company required during data collection process.

This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and reputed company yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time. Apply tot his job Apply To this Job