Your main responsibilities as a Clinical Research Associate II: Support study team with clinical trial management activities including protocol review, da Clinical Research, Research Associate, Clinical, Associate, Research, Healthcare, Staffing. R&D Partners is seeking to hire a Clinical Research A...
The Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
Clinical Research professional to assist with the design and implementation of in vitro function registration studies utilizing healthy subjects. Assists Early Clinical Development and Regulatory Affairs with clinical trial submissions and updates. BS or equivalent with a minimum 5 years of experien...
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...
As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and th...
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 ...
The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Works under the direction of a Clin...
The Clinical Research Coordinator (CRC) will be responsible for providing clinical and administrative support to the Principal Investigator (PI) for a variety of research studies conducted in the SFVAHCS Cardiac Catheterization Laboratory (CCL). The CRC will be responsible for the coordination of on...
A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Study Lead for a hybrid role in San Francisco (Palo Alto). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases I...
The incumbent will serve as a Staff Research Associate III/Clinical Research Coordinator for various project and will provide compliance oversight and day-to-day study coordination activities as assigned by the Manager of Compliance and Contracts. The Clinical Research Coordinator (CRC) is a special...
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 Lead Clinical Research Associate manages the design, execution, and monitoring of internal and external clinical studies, coordinates the development of operating procedures, coordinates in the development of standard procedures in executing experiments, evaluation, and documentation of results,...
Under the supervision of Principal Investigator (PI), the clinical research coordinator (CRC) will perform duties related to the support and coordination of clinical research studies and may receive training and development to prepare and advance for journey-level work at the next level within the s...
Supporting study operational activities under the direction of the clinical study lead. ...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
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. ...
The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial man...
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. ...
Staff Research Associate II or III. The Cyster lab has an exciting opportunity for an SRA 2 or 3 to join the research team. The overall purpose of this position is to be an integral part of the Cyster lab research team working with other lab members on a range of immunobiology studies as the 'point ...
Under the guidance of the principal investigator, the assistant CRC will follow protocols for study initiation; collect data to complete research data forms based on source documents; gather and interpret medical, surgical and laboratory data regarding clinical trial subjects after training with the...
The UCSF Fresno Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and Principal Investigators (PIs); may coordinat...
Under the supervision of a Clinical Research Supervisor or Principal Investigators (PIs), the Assistant Clinical Research Coordinator will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journ...
The Assistant Clinical Research Coordinator (Assistant CRC) works directly with the Principal Investigator (PI) and performs duties related to the support and coordination of research. Assistant Clinical Research Coordinator - Neuroscape Center. The Neuroscape Center at UCSF is looking for an Assis...
The University of California, Berkeley, is one of the world's leading institutions of higher education, distinguished by its combination of internationally recognized academic and research excellence; the transformative opportunity it provides to a large and diverse student body; its public mission ...
It has direct responsibility for implementing a diverse portfolio 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 programmatic clinical research activities, such as a ...