Participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelors degree with 4+ year experience as a Clinical Trials Asso...
Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Monitors activities conducted by clinical investigative ...
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...
The Clinical Research Informatician is a bridge between clinicians/researchers and data. They blend their knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care. Cl...
The Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Two years: Experience in a Clinical Research setting. F02 AMG Clinical Trials: Required to have College Degree. Upon hire: Phlebotomy Certificate (for department SJuHMG Clinical Trials). ...
Working under direct supervision, the Research Associate I performs a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. Are you ready to be a part of breakthrough research?. Maintains compute...
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...
Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure the efficient and compliant clinical operation of the Early Phase Clinical Unit (EPCU). Parexel Early Phase Clinical Unit. Develop professionally by gaining experience in delivering high-qua...
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...
Assist in the coordination of Phase I-IV clinical trials. ...
The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies. Provide clinical research support to investigators to prepare for and execu...
CeASES-ADRD is an interdisciplinary research center supporting innovative research on the health, economic and social impacts of dementia by identifying opportunities to reduce risk and costs of dementia, improve access and care, and advance solutions for achieving health equity. A collaboration of ...
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 ...
Manage Clinical studies as Project Owner for all assigned studies, as outlined in the Clinical Studies process, with accountabilities/authorities specified in the process map including ensuring protocol and study design are feasible, develop and train team on the project plan, risk mitigation plans,...
Bachelor's Degree with 2-3 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is required. Maintain and expand communication with clinical partners to raise awareness of the warmline. Monitor and evaluate the delivery of car...
The Clinical Research Associate I will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support. Bachelor’s degree in a clin...
The USC Norris Comprehensive Cancer Centers Clinical Investigations Support Office (CISO) is seeking an Assistant Director, Clinical Research Operations to join its team. Job Summary: Provides oversight, supervision, and support for research operations, processes, and infrastructure related to clini...
Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training. Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and ...
The Clinical Research Associate II will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for external sponsors. Schedules research participants ...
The ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or progr...
Job Description Are you looking to contribute to groundbreaking research? We look forward to having you join our team to collaborate on groundbreaking research! The Clinical Research Specialist provides clinical research expertise by participating in the design and implementation of research project...
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 ...
Facilitating and supporting studies and research as needed. ...
Promote good clinical practice in the conduct of clinical investigations, included possessing an in-depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Coordinate and conduct clinical studies, includes; subject recruitme...
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 Clinical Research Coordinator contributes to the overall operational management of ...