Minimum two (2) years of experience in clinical protocols involving research methodology/research study design, and hypothesis testing. May coordinate research project activities with other research study centers. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Min...
A company is looking for a Clinical Research Associate II. ...
Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Monitors activities conducted by clinical investigative ...
Key Responsibilities:Lead business development and capture for opportunities within federal agenciesDirect and manage large clinical trials support services contracts or projectsMentor a team of clinical research professionals and foster a culture of continuous improvementRequired Qualifications:Mas...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
A company is looking for a Senior Director, Clinical Research to lead clinical research programs in nephrology, rheumatology, and infectious diseases. Key Responsibilities:Serve as an independent Medical Monitor for clinical trials from Phase 1 through Phase 3Provide oversight and medical accountabi...
Ability to interact with the Clinical Research Supervisor, Clinical Research Coordinators, independent contractors (i. DescriptionThe Clinical Research Nurse is a professional caregiver who assumes responsibility and accountability for a group of patients for a designated time frame and provides car...
The Clinical Research Associate I will function under the supervision of the Clinical Research Supervisor, coordinating and maintaining diverse activities related to clinical trials at the John Wayne Cancer Institute. Clinical research coordination, or 2 years of clinical research data entry or equi...
The Clinical Research Data Specialist II manages the data for assigned research studies. In addition, may train clinical research staff, perform basic statistical analysis, and work with bioinformatics to develop and maintain trial management systems. May train clinical research staff to help improv...
The Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Two years: Experience in a Clinical Research setting. F02 AMG Clinical Trials: Required to have College Degree. Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials). ...
The CRA I member works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. In the Slomka Lab, the primary duties of the Clinical Research Associate I are to coordinate and help implement research study activities ...
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...
It's crucial to maintain awareness of regulatory changes, technological advancements, clinical and research processes, and standards of clinical research conduct. The USC Norris Comprehensive Cancer Center’s Clinical Investigations Support Office (CISO) is seeking a Clinical Trials Reporting Program...
A minimum of 2 years clinical research experience (either as a high-achieving research coordinator or CRA). RDI is seeking a Senior Clinical Associate to ensure our clinical trials are completed on-time, according to the protocol, and keeping our clients and sites informed throughout the process. Kn...
Under the supervision and guidance of the department leader and/or seasoned analysts, the Departmental Application Analyst I is responsible for day to day efforts involved in the resolution of interrelated departmental applications and reporting issues associated with the departmental applications a...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential 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 ...
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...
Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. The Clinical Research Coordinator contributes to the overall operational management of ...
As a Clinical Research Coordinator III, you will work independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This position is res...
The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or progr...
Job Description Grow your career at Cedars-Sinai! Join our team and use your skills with an organization known nationally for excellence in research! This position functions as a Clinical Research Finance Coordinator (CRFC) responsible for coordinating and executing the financial billing of clinical...
Overview Purpose Statement/Position Summary: The Clinical Research LVN manages all aspects of research protocols and clinical trials. Clinical Research experience preferred. Here world-class experts in medicine, education and research work together to deliver family-centered care half a million time...
The Clinical Research Informatician is a bridge between clinicians/researchers and data. Must have a blended knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care....
The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (CTOM...
Title: Clinical Research Associate. REQUIRED EXP: Min 2 yrs exp in a clinical research coordinator role with recent experience being in an Academic Medical Center. ...