Clinical Research Coordinator II - Pulmonary Research Program/Lung Institute. As a Clinical Research Coordinator II, you will work independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and par...
The goals of the fellowship are (1) identification of appropriate areas of research activities, (2) research methodology and experimental design, (3) preparation of grant proposals, (4) scientific writing: preparation of abstracts for scientific meetings and manuscripts for peer review journal publi...
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Works with a Clinical Researc...
The Clinical Site Manager will assume a leadership role in overseeing all clinical research activities at the designated site, including industry-sponsored studies and investigator-initiated studies. This individual will manage multiple study managers, clinical research coordinators (CRC), research ...
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal w...
As a Sr CRA you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a ...
Exciting opportunity for a detail-oriented individual! Join us as a Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol. Join the forefront of groundbreaking research at theBeckman Resear...
Broad-based research plays a critical role in the care of our veterans through scientific investigations relevant to the diagnosis, delivery of care, clinical practice, and treatment of diseases affecting veterans. This unique opportunity will work closely with UCLA residents and fellows and is supp...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
Desired skills include:Clinical research Dosage ranges Indications Ethical ResearchPrinciples & Practices Side effects Keen attention to detailMedical terminology Microsoft Office proficiency Licensing orCertifications for Clinical Research Nurse and Physician AssistantList any licenses or certifica...
Extracts and enters required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs). The USC Institute of Urology is seeking for a part-time clinical research data specialist I to facilitate and manage the urologic clinical data for assigned pr...
We are seeking a Clinical Research Coordinator with a minimum of 2 years of experience in a clinical research setting. Job Title: Clinical Research Coordinator. Minimum 2 years of clinical research experience. ...
The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values. Profound enables community physicians to offer clinical research a...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Join our team and use your experience with an organization known nationally for excellence in research! The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Primary Duties an...
As a Clinical Research Specialist I, you will provide clinical research knowledge by participating in the design and implementation of research projects as needed. Are you looking to contribute to groundbreaking research? We look forward to having you join our team to collaborate on groundbreaking r...
The company offers a great work environment!Clinical Research Coordinator Pay and Benefits: * Hourly pay: $30/hr* Worksite: Leading hospital and health care system (Los Angeles, CA 90045 - Hybrid)* W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL* 40 hours/week, 4 ...
The Clinical Research Informatician is a bridge between clinicians/researchers and data. They blend their knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care. Cl...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Primary Duties and Responsibilities• Works with a Clinical Research Coordinator, Research Program Administrator or Resear...
A global role reporting into Senior Manager, Clinical Research Pharmacy Services supporting IP Management specific deliverables in Clinical Trial Execution. Broad work experience in life sciences or medically related field, including biopharmaceutical clinical research experience working on clinical...
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...
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research methodol...
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for compl...
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 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 ...