Do you have a passion for the highest clinical quality and patient happiness? Would you like to use your clinical competencies with an organization known nationally for excellence in cancer treatment, research and education? We would be happy to hear from you! Please consider the following exciting opportunity with one of the most outstanding and dynamic places to work in the medical field as your next career move.
The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. We are committed to bringing innovative therapeutic options to all those we serve with cancer. You can look forward to working closely with our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists to advance cancer care.
As a Clinical Research Coordinator, you will provide support for clinical research protocols for the department and assist with all aspects of clinical research. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements.
Summary of Essential Duties:
Responsible for administrative functions of research studies.
Maintains comprehensive knowledge of assigned research protocol to coordinate the comprehensive and compliant execution of assigned protocols in accordance with research governing entity requirements, including but not limited to Sponsor, FDA and IRB requirements.
Works with PIs and Research Nurses to ensure the completion and maintenance of consent forms, case report forms, SAE's and source documents to ensure that research is being conducted according to FDA, HSPC, HIPAA and other agency guidelines
Reviews protocols and informed consent forms for completeness and compliance with regulations.
Reviews all clinical study records including informed consents, to ensure complete documentation in compliance with regulations.
Assists in the preparation of new protocols.
Coordinate and follow all protocol related procedures.
Coordinate with data managers for completion of case report forms (CRF's) and data entry for clinical research projects as needed.
Provide support (including administrative/clerical) and information to subjects, staff, and external sources related to current research projects.
Maintain scheduling of pre-study testing, treatments, outside labs, scans, biopsies and other tests for all clinical research visits.
Attend meetings and conferences related to research activities.
Act as liaison and coordinate efforts with other departments and personnel.
Maintain research charts and subject records have proper source documentation.
Obtain follow up information and reports for all subjects on study.
Obtain medical records, death certificates and death information for all subjects as needed.
Follow up subjects as needed by telephone, to insure compliance with treatment guidelines.
Interact appropriately with other members of the clinical team and office personnel, communicating in a highly professional manner at all times.
Maintain appropriate records of clinical activities.
Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested.
Establishes and coordinates logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
Acts as a liaison with Principal Investigators, pharmaceutical company representatives or other project funding organizations to monitor and update project progress.
Facilitates patient screening, recruitment and scheduling, initiating research patient records, administration of questionnaires, maintaining database Excel spreadsheets, completion of case report forms, performing data edits with P.I.'s research staff, pharmaceutical company monitors, etc.
Protects rights and research data of research volunteers, including medical records, data, etc. Obtain necessary consent forms, or HIPAA information forms as needed, in research process.
Providing healthcare for more than 100 years, Cedars-Sinai has evolved into one of the most dynamic and highly renowned medical centers in the world. Along with caring for patients, Cedars-Sinai is a hub for biomedical research and a training center for future physicians and other healthcare professionals. This attracts exceptional talent to Cedars-Sinai, including world-renowned physician-scientists who seek a place where they can both conduct research and see patients--the ideal formula for discovery and its translation into cures. Our patients benefit from access to doctors at the top of their fields, and our researchers have an ideal community in which to study the impact of healthcare challenges, and reflect that knowledge in their research. The greater Los Angeles area in which Cedars-Sinai resides possesses unparalleled cultural and ethnic diversity which offers outstanding opportunities for translational and clinical research... and a dynamic environment for medical education.Although community based, Cedars-Sinai is a major teaching hospital affiliated with the David Geffen School of Medicine at the University of California, Los Angeles (UCLA). Cedars-Sinai has highly competitive graduate medical education programs in more than 50 specialty and subspecialty areas, a graduate program in biomedical sciences and translational medicine, a clinical scholars program directed towards junior physicians with aspirations to become clinical scientists, and post graduate training opportunities.There are more than 250 full-time faculty members at Cedars-Sinai. The voluntary medical staff, comprised of more than 2,200 specialty board-certified or board-qualified physicians, represent all of the specialties and subspecialties and collaborate with full-time medical staff in the teaching responsibilities of the graduate medical education programs.