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...
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...
Under supervision of the Clinical Research Manager of the Clinical Trials Unit, the Assistant Clinical Research Coordinator supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management of multiple Phase II-IV cancer-related protocols accordi...
UCI Stem Cell Research Center - Alpha Clinic (UCI AC): The UCI AC provides the necessary infrastructure, clinical, and operational expertise to accelerate cell and gene therapies clinical trials at UCI. Under the supervision of the Assistant Director (AD), incumbent is responsible for coordinating r...
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...
Under the supervision of the Assistant Director of Business Development & Technology, incumbent is responsible for managing recruitment of potential research participants for clinical trials at the UCI Center for Clinical Research, within Good Clinical Practice (GCP) guidelines. The UCI Center for C...
A large medical device company located in Irvine, CA is looking for a Clinical Study Associate to support the planning, executing, and management of clinical trials. Coordinate and manage logistics for clinical trials. Maintain study files and documentation in accordance with Good Clinical Practice ...
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...
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...
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...
Primary Schedule: Wednesday - Sunday 9:00pm - 5:30pmWhy CenExel ACT? Be part of one of the largest and fastest-growing clinical research companies in the United States with potential internal growth and advancement Work alongside a successful and dynamic team conducting clinical trials for new medic...
The AoUSCC led by UCI is a part of the larger research structure for the All of Us Research Program and the Genetic Epidemiology Research Institute (GERI) efforts including UCI faculty and researchers in furthering the science of precision medicine using the All of Us data. Broad knowledge of clinic...
Under the direction of the Program Manager, the Assistant Clinical Research Coordinator supports the research efforts of several regional projects. Preferred: Master's degree and/or experience in public health or clinical research. The campus has produced five Nobel laureates and is known for its ac...
Review, identify and investigate discrepancies in study documentation by applying clinical protocol and GCP knowledge and develop processes to mitigate reoccurrence throughout study phases• Assist with facilitating recurring study team meetings and external site communications• Partner with cross-fu...
The Clinical Research Field Monitor is responsible for compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. Experienced with Good Clinical Practice (GCP) in conduct of clinical studies. Preferably certified as a Clinical Research ...
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. ...
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...
This professional will report to Clinical Science and External Research (CSER) Leaders in the management of assigned clinical projects for the Cardiovascular Group to support the development of the evidence generation and dissemination strategy of assigned products, manage clinical studies, execute ...
The Clinical Research Regulatory Coordinator will support clinical research teams (physicians, nurses, etc. Will serve as a central resource for staff conducting clinical research. This position reports to the Director, Clinical Research. Remains informed of current federal, state, and local regulat...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
As a Clinical Research Physician/ Neurologist you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. Your role will be focused on phase I-IV clinical trials, where you will be responsible for assessing and following the safet...
The Clinical Research Regulatory Supervisor assists in overseeing clinical research regulatory operational activities. Is responsible for conducting clinical research to industry standards and best practices. Assists with ensuring proposed projects meet the mission and vision of Client and all Clini...
The Contracts & Grants Analyst will effectively use available resources to ensure the accuracy of research accounting records and address financial issues to secure the continued success of SJHH research. Under the supervision of the Director, the Contract & Grant Financial Analyst is responsible fo...
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 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 ...