A company is looking for a Clinical Research Associate II. ...
Calling all infusion, emergency, and clinical research Registered Nurses!! Are you looking to expand your skillset? Would you like to help to bring life changing medicines to patients faster! Are you looking for a flexible opportunity to enhance your monthly income?. Unique and varied clinical exper...
A company is looking for a Clinical Research Specialist in Oncology. ...
Responsible for the coordination of study activities, the collection and delivery of study data, and the communication between investigators, study team, and sponsor; interact closely with investigators, sponsors, monitors, regulatory/budget/contract Clinical Research Associates (CRAs), and Institut...
A company is looking for a Clinical Research Coordinator for a Clinical Trials Processing Lab. ...
The Clinical Trials Coordinator is responsible for facilitating all aspects of clinical trials within the Providence Brain and Spine Institute. Bachelor's Degree - Health related field with 3 years in clinical research experience or,. ...
Responsible for ensuring accurate, quality data collection, protocol interpretation: carry out complex procedures, medication administration, and compliance in specialized areas of clinical research. Perform all duties and responsibilities of the Clinical Research Specialist III. Minimum three (3) y...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
The Clinical Applications Principal Architect is responsible for developing the architectural design of Clinical software applications and directs the technical team throughout the design and development of build in Epic and other clinical applications. Jude Children’s Research Hospital consistently...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum...
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. Minimum of 1 year of clinically-related experience, of w...
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 Monitor supports clinical research studies by monitoring protocol and regulatory compliance, reviewing research data for accuracy, managing documentation and milestones, auditing essential documents, writing monitoring reports, and developing risk monitoring plans and study-rel...
This TI clinical research assistant II position will support study coordination for several clinical trials and infectious disease epidemiological studies focused on the natural history of NTM, HIV, yellow fever, and other infectious diseases. A working knowledge of FDA, DHHS, IRB and other agency g...
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 OHSU Knight Cancer Institute Sr Clinical Research Assistant (formerly Data Manager), is responsible for the collection, entry, and general management of oncology study data for oncology clinical trials. Primary duties include ensuring accurate and complete research data is collected from oncolog...
Position at Premier Research Premier Research is looking for a Manager of Clinical Quality Operations to join our Corporate Quality team. Premier Research is more than a company – it’s a community of people that truly care about one another, about our clients, and about our mission of furthering res...
The Oncology Clinical Research Supervisor will lead clinical research activities within their designated OHSU Knight Cancer Institute clinical research program(s). In support of these activities, the Clinical Research Supervisor is involved in continual process improvement to further the efficiency ...
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. Precision’s uniquely integrated offerings enable the science of precision...
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. Minimum of 1 year of clinically-related experience, of w...
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 Lead-Clinical Research Associate is responsible for performing data abstraction, collection, and entry to support clinical research. Provide clinical operations expertise to inform clinical trial operational feasibility and delivery, and development of study recruitment and retention strategies....
The Clinical Coordinator works directly under a directors for the Center for Embryonic Cell & Gene Therapy (CECGT) Principal Investigators (PI) and/or Research Manager and will be responsible: for the conduct of clinical research with human participants; the development and/or management of regulato...
The SHS Research Institute includes the Human Research Protections Program, Sponsored Program Administration, Clinical Research, Research Administration and Research Development Offices. Coordinates and monitors patient’s care while participating in clinical research studies. These departments work ...
The Clinical Research Coordinator I will function under the supervision of the Clinical Trials Manager. Coordinates and maintains diverse activities in the conduct of clinical research trials related to heart and vascular research. Experience with clinical research. Bachelor's or Associate's Degree ...