Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements. Provide guidance and training to clinical research staff. Perform clinic...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal 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. Works closely with a regulatory coordinator or directl...
ABA Clinical Coordinator (Program Supervisor). Provide clinical training and support to a dedicated team. ...
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. Works closely with a regulatory coordinator or directl...
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 Services Coordinator, Intermediate (CSC) will report directly to the supervisor of care management support operations and will serve as initial point of contact for providers and members in the medical management process by telephone or correspondence. ...
Are you ready to bring your clinical skills to a world-class facility recognized as top ten in the United States for transplant services? Do you have a passion for the highest quality and patient satisfaction? Then please respond to this dynamic opportunity available with one of the best places to w...
The Clinical Services Coordinator Intermediate will report to the CHP Manager. The Children’s Health Program (CHP) team provides identification, referrals, and care management for all Medi-Cal members under years old and collaborates within Promise Clinical Team. In this role you will work with cli...
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...
High-Throughput Screening Research Associate I, II, III. Founded by pioneers in the CRISPR field from leading institutions for gene editing research, the company is developing a first-of-its-kind RNA writing platform that can correct thousands of bases at once, thereby correcting genetic mutations s...
As a Senior Research Associate, you will be responsible for developing and optimizing HPLC methods, conducting qualitative and quantitative analyses, and supporting various research and development projects. Perform routine and advanced HPLC analysis to support research and development activities. T...
Reporting to our Associate Director of Clinical Operations, the. Prepares and maintains documents and files such as clinical study files, regulatory binders, and operations manuals for clinical sites (i. Has some understanding of the science behind Clinical Research, observes and gains exposure to c...
Research Associate, Bioanalytical Development. ...
We are partnered with a growing gene therapy startup in South San Francisco seeking a highly skilled Senior Research Associate of Nucleic Acid Analytics to support to support research across RNA and DNA analysis. Support research through analysis of RNA and DNA, characterizing gene therapy vectors. ...
Avania is hiring Senior Clinical Research Associates (Sr CRAs) - West Coast - Extensive cardiology Class III device monitoring experience required. Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
Likewise, since entering the project development business in 2010, Canadian Solar has developed, built, and connected over 9 GWp of solar power projects and over 3 GWh of battery storage projects across the world. Currently, the Company has approximately 700 MWp of solar power projects in operation,...
Are you an experienced Project Coordinator with a desire to excel? If so, then TALENT Software Services may have the job for you! Our client is seeking an experienced Project Coordinator to work at their company in CA(100% remote). Familiarity with Planview or similar project management software. ...
Job Summary: The Project Coordinator / Administrator will assist in the bidding process and provide administrative support to the project team in planning, organizing, and managing construction projects from inception to completion. SoCal General Contractor specializing primarily in Industrial Concr...
A priority client of Insight Global is looking for a qualified Project Manager with the ability to work in a very high paced environment. ...
As a PMO Project Manager at MP, you will be responsible for driving the successful implementation of Project Management Offices within client organizations. Every day, we support our clients by steering major Projects and Programs, managing Project Portfolios, improving maturity and efficiency of PM...
Develops research project budgets based on protocol requirements and Cedars-Sinai published research costs, ensuring that all anticipated costs are appropriately accommodated and that research protocol, research budget and research subject informed consent documents are consistent. The Research Asso...