The Coordinator-Admin Research is responsible for coordinating and facilitating research in the department and includes activities undertaken by attending physicians, residents, and medical students. This position will also be responsible for overseeing research cost with department administration a...
Job Title: Clinical Research Coordinator. We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. The Clinical Research Coordinator will be responsible for supporting the planning, implementation, and coordination of clinical trials conducted wit...
The Assistant Coordinator-Oncology Research serves as regulatory assistant and administrative support for the Oncology Clinical Research department in order to facilitate the implementation and management of oncology clinical trials, assists in document preparation and maintenance for study mandated...
Clinical Research Coordinator (sponsor-backed trials) Highly Preferred BA/BS in a scientific discipline. We are a global Clinical Research Institute that has been conducting Clinical Trials over the last 25 years. ...
Coordinator-Clinical Research 3 is responsible and accountable to oversee and coordinate the implementation and management of research trials. Certified Clinical Research Coordinator (SoCRA, ACRP) required within six months of hire date required. Our mission is to participate in Jesus Christ's minis...
The Clinical Research Coordinator II is crucial to the companies clinical research, managing multiple complex trials across various areas and phases. An exciting Clinical Site Network are looking to bring on board a Clinical Research Coordinator to either of their sites based out of. Minimum of 3+ y...
The Coordinator-Admin Research is responsible for coordinating and facilitating research in the department and includes activities undertaken by attending physicians, residents, and medical students. This position will also be responsible for overseeing research cost with department administration a...
Association of Clinical Research Professionals Certified Professional (ACRP-CP), Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC). Preferred: Clinical research experience in a hospital setting and/or pediatric clinical research experience. Required: M...
The Clinical Research Coordinator II works independently providing study coordination including 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 e...
Under moderate supervision, the Clinical Research Coordinator I (CRC-I) is expected to perform all core Clinical Research Coordinator (CRC) responsibilities for human subjects’ (clinical) research. Study management includes but is not limited to assisting in assessing feasibility of clinical researc...
Conduct research and evaluation activities per CEPA's Research and Evaluation department, includes but not limited to the following:. Under the leadership of the Center for Equity and Postsecondary Attainment Directors, the Grade Level Coordinator will work in person, directly with students to provi...
Coordinator-Clinical Research 3 is responsible and accountable to oversee and coordinate the implementation and management of research trials. Certified Clinical Research Coordinator (SoCRA, ACRP) required within six months of hire date required. Our mission is to participate in Jesus Christ’s minis...
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...
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 ...
Title: Clinical Research Coordinator, On-Site . Clinical Research Coordinator experience within a similar setting preferred . Obtains informed consent of research subjects . Performs patient/research participant scheduling . ...
The Coordinator-Clinical Research 2 assists with and coordinates activities associated with clinical research conducted by LLUHC. Coordinates care, screening, recruitment, research exams, medical record review, and data entry; prepares study related documents as outlined by the research protocol. Ce...
Research high-quality software user audiences and identify new methods to generate reviews. ...
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 Senior Research Assistant assists in entering and maintaining all documentation and records. Minimum two years of administrative/clerical experience required; one year research or laboratory experience preferred. Completion of LLU's educational program on "ethical use of human subjects in resear...
The Coordinator-Clinical schedules patients, CBCT acquisitions, other image acquisition as indicated and report productions, also includes standard functions of greeting, positioning and dismissing patients, and assisting faculty with imaging related functions. ...
The Research Assistant supports the execution of certain aspects of a research project after the research design is established with minimal supervision. Able to read; write legibly; speak in English with professional quality; use computer, printer, and software programs necessary to the position; A...
Relevant experience may be Project Engineering Manager, Senior Structural Engineer, Structural Engineering Manager, Principal Engineer, Principal Engineering Manager, Senior Project Engineer, Senior Engineering Project Manager, Engineering Project Manager. The ideal candidate will be a Licensed Engi...
The Senior Clinical Research Associate will report to Manager, Clinical Affairs, and will play a key role to proactively support the conduct of pre-market and post-market clinical studies to ensure compliance with all the regulatory requirements. Contribute to all clinical research activities to ens...
Our team is seeking one full-time Study Operations Assistant to support a large-scale military research program at the Naval Health Research Center in San Diego. The position will work closely with the Survey Operations teams to execute funded research projects that collect data from servicemembers ...
As a Research Associate in the Medicinal Chemistry group, you will join a comprehensive, interdisciplinary research team dedicated to making significant advances in discovering vital new drug candidates. Research Associate, Medicinal Chemistry. Plan and execute assigned experiments to support resear...