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...
This position will have an integral role in protecting the health, safety, & welfare of research participants having a thorough knowledge of clinical research protocols and collaborating and the clinical research team including clinical research coordinators and research pharmacists. This position i...
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 candidate will help coordinate among Clinical Research Coordination team members conducting investigational clinical studies in accordance with Food and Drug Administration (FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures. Become an expert u...
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...
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 ...
Clinical Research Specialist located in Irvine, CA. Job Description: Serves as an expert on clinical trial matters and provides governance on clinical trial operations. Utilizes clinical trial best practices to ensure the safety and confidentiality of all study subjects in clinical activities. ...
The CRC II may assist with the training and/or mentoring of CRC I or other CRC II staff on the basics of clinical research, Good Clinical Practice (GCP), Good Documentation Practices (GDP), Standard Operating Procedures (SOPs) and other related aspects of the clinical study. Responsible for the over...
The RNC provides support, coordination and leadership for FDA regulated research including drug/device/biologic studies that may involve industry sponsored Phase I, II, III and IV clinical trials, government funded clinical research and investigator initiated clinical research. The Research Nurse Co...
Clinical Research Coordinators need to engage with research subjects, explain what is expected of them and understand their concerns, requiring excellent interpersonal and communicative skills. We are looking for candidates with medical backgrounds and excellent interpersonal skills for the position...
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 ...
Fosters and maintains collaborative relationships between patients, their family/support group, physicians, and other healthcare providers Clinical Research, Nurse, Oncology, Hematology, Clinical, Research. Is responsible for all aspects of clinical research performance, under the supervision of the...
Your Role on the Team Under the supervision of the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). The UCI Center for Clinical Research (CCR) is driven to improve health and wellness of p...
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. Plan, implement and conclude clinical studies in support of project timelines/market rel...
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...
We are seeking an experienced and detail-oriented Clinical Research Coordinator (CRC) with at least 2 years of experience in clinical research. At least 2 years of experience as a Clinical Research Coordinator or in a similar role. Coordinate and manage clinical trials from start-up to close-out, en...
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...
Under the supervision of the Assistant Director of Clinical Research Operations, the incumbent is responsible for coordinating clinical trials in the UCI Center for Clinical Research (CCR). The UCI Center for Clinical Research (CCR) is driven to improve health and wellness of people in Orange County...
The goals of the fellowship are identification of appropriate areas of research activities, research methodology and experimental design, preparation of grant proposals, scientific writing: preparation of abstracts for scientific meetings and manuscripts for peer review journal publication and admin...
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...
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...
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...
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...
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 ...
The Clinical Research Regulatory Supervisor assists in overseeing clinical research regulatory operational activities. Position Title: Clinical Research Regulatory Supervisor. Is responsible for conducting clinical research to industry standards and best practices. Assists with ensuring proposed pro...