Under supervision of the Clinical Research Manager, the Assistant Research Data Coordinator (ARDC) supports the clinical research efforts of the CFCCC by providing comprehensive data management for a research portfolio of Phase I-IV cancer-related protocols according to Good Clinical Practices (GCP)...
Minimum 1 year of experience in previous study coordination or clinical research coordination. Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GCP) for clinical research. Working knowledge of the clinical research regulatory framework and institutional requ...
Under the supervision of the Clinical Research Manager, the Long-term Follow-up Clinical Research Coordinator (LTFU CRC) supports the clinical research efforts of the Cancer Center by providing comprehensive patient coordination and data management of the long-term follow-up requirements for complic...
Req ID : HRC1394612 Working Title : Clinical Research Coordinator I - Smidt Heart Institute Department : Heart Institute Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shift : Day Shift...
Under the direction of the Director of Health Systems Science (HSS) Research Operations, the Research Coordinator will provide research coordination and project management for the HSS. Provide study coordination and project management for several research awards, including coordination for all study...
Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Two years experience in a Clinical Research setting. ...
Training Coordinator is a business-critical role to ensure that clinical trials are conducted according to local regulations, international guidelines, SOPs, and protocols by coordinating and performing, where appropriate, awareness, orientation, and skills training for all staff. Highly preferred 1...
Coordinate and conduct clinical studies, includes; subject recruitment, informed consent, chart maintenance and data entry.Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.Assure compliance with the protocol and regulatory requirements includes: collecting, recording...
We’re seeking a self-motivated, independent professional with: * Five or more years of experience as a study coordinator for clinical research * Data management experience with clinical research protocols * Knowledge of health services or clinical research methodology and principles * IRB experience...
The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies. We are seeking a motivated and detail-oriented Research Coordinator to join...
We’re seeking a self-motivated, independent professional with: * Knowledge of health services or clinical research methodology and principles * Computer proficiency with Microsoft Word/Excel/Publisher/Access * In-depth understanding of Human Subject Protection and informed consent * Experience follo...
Join UCLA Health and play a pivotal role in cutting-edge medical research. Play a key role with a world-renowned leader in medical research. You will develop summary tables and enter data into a dynamic database to provide the research team with a vital layer of precision for their critical work. Th...
Overview Position Summary: The Clinical Research Coordinator III, as a certified research professional, handles clinical trial administration for all protocol phases for the Leukemia and Lymphoma Disease department. ACRP Certified Clinical Research Coordinator (CCRC) or SoCRA Certified Clinical Rese...
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Work alongside physician-scienti...
Under the direction of the Manager of Development Operations, this position supports the Development Department in which principal responsibilities include researching, analyzing and providing high-level research on high-net-wealth individuals, corporations and foundations using a variety of biograp...
The Clinical Research Coordinator II works independently providing study coordination including screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Req ID : 1696 Working Title : Clinical Research Coordinator I - Alzheimer's and Dementia Research Program - Department of Neurology (Hybrid) Department : Research - Neurology Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial...
Overview Position Summary: The Clinical Research Coordinator II, as a certified research professional, handles clinical trial administration for all protocol phases. ACRP Certified Clinical Research Coordinator (CCRC) or SOCRA Certified Clinical Research Professional (CCRP) required. Here world-clas...
Consent patients and coordinate visits, lab blood draws and tissue acquisition.Collect, process, and ship biospecimens.Abstract data from electronic medical records.Accurately and efficiently enter data into REDCap.Assist in the creation, organization, and maintenance of spreadsheets and databases.A...
The Clinical Research Budget Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time, ...
The Clinical Research Finance Coordinator I develops clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. Evaluates research protocols to assess resource needs for research procedures, clinical research staff time, investigator time,...
Clinical Study Coordinator - Clinical Research (On-Site). Duarte Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials. Under the supervision of the Director, Clinical Research, this patient-facing role involves coordinating First in Human to Phase ...
As a Study Coordinator in clinical research, you will be responsible for human subject recruitment, screening, enrollment, and retention. Five or more years of experience as a study coordinator for clinical research. Play a key role with a world-renowned leader in medical research. Data management e...
Establish and maintain relationships with targeted organizations and utilize those relationships to strategically implement the continued care model, placing patients into longitudinal treatment within the community.Maintain a vast understanding of multiple pathways to wellness including harm reduct...
The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities. The Assistant Clinical Research Coordinator recognizes and performs nec...