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....
The CTRC supports innovative, patient-oriented research, offers clinical research training and recognition programs and provides researchers an environment for seeing patients when they take part in clinical research studies. Provides clinical research nursing support and patient care in an outpatie...
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 Specialist I provides clinical research expertise by participating in the design and implementation of research projects as needed. Provides clinical research expertise by participating in the design and implementation of research projects as needed by the department or institu...
Extracts and enters required clinical data from medical records and patient research charts/reports into Clinical Research Forms (eCRFs/CRFs). Clinical Research Data Specialist II. Coordinates and manages the clinical data for various phases of clinical study. Acts as primary site contact with spons...
This position is responsible for leading clinical research staff for clinical activities in support of new and existing Diabetes products and therapies to achieve regulatory approval and establish comprehensive clinical evidence, by optimizing clinical trial process, its infrastructure setup and sup...
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 Department of OBGYN is seeking to hire a full time Clinical Research Coordinator to...
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. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
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 Research Professional (CCRP). M...
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....
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...
Senior Clinical Research Associate positions open for a Biotechnology client. The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating p...
Responsibilities : The Department of Medicine Clinical Trial Program is seeking a skilled Clinical Research Associate to oversee, manage and participate in research activities. Providing oversig...
Req ID : HRC0519690 Working Title : Clinical Research Coord I - Smidt Heart Institute / Barbra Streisand Women's Heart Center (BSWHC) - Bairey Merz Lab Department : Heart Institute Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin...
Overview Position Summary: The Clinical Research Coordinator I, per-diem assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Certified cli...
The Research Administrator is the Institutional representative for sponsored cancer clinical trials and is the primary point of contact for sponsor and University clinical research grant and contract administrators. The SCI Clinical Trials Office (SCI CTO) is an integral component of the Stanford Ca...
Finance Manager, completes operational budget and financial analysis to determine opportunities for cost savings, appropriate pacing of initiative spending and proactive cash flow predictions for the senior financial administration of the health system.Incumbent will support the department managers,...
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. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement stud...
Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Clinical Research Associate (Sr. Minimum of five (5) years in clinica...
The Clinical Research Associate I will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. The inc...
Highly preferred 1-2 years related experience in clinical research. Parexel Early Phase Clinical Unit. 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 perfo...
Overview Purpose Statement/Position Summary: The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Certi...
The Accelerated Program of Education, Exposure, and Experience for Clinical Research Associates (APEX CRA) provides foundational clinical research training including project and system experience. Do you have up to 2 years of experience working as a Clinical Research Coordinator in Ophthalmology or ...
Research, Good Clinical Practice (GCP), Federal Regulations pertaining to research, and applicable guidance’s and regulations. USC Norris Comprehensive Cancer Center - CISO is seeking a Clinical Research Program (Disease Team) Manager. Supervises – Disease Team Study and Research Coordinators who pr...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...