Clinical Research Associate (SCRA) on a hybrid capacity in their SF office. Working with a precision IO biotechnology company to build out their clinical operations team and they are currently looking for a Sr. Supporting study operational activities under the direction of the clinical study lead. ...
Clinical Research Associate (CRA/Senior CRA for In-House Opportunity). Participate in providing guidelines for assessing the adequacy of potential clinical investigators and sites: including evaluating facilities, personnel, patient referral base, and adherence to Good Clinical Practices (GCP). Part...
The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. ...
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...
As our research assistant you will be primarily responsible for assisting in research patient visits according to ICH-GCP guidelines and according to the IRB-approved study protocol and/or manual of procedures. Prepare visit-specific documentation and charts for Clinical Research Coordinator. Throug...
Contribute to all clinical research activities to ensure successful management of clinical studies under the direct supervision of Clinical Affairs manager with dotted lines to clinical study manager. The Senior Clinical Research Associate will report to Manager, Clinical Affairs, and will play a ke...
The Director of Clinical Research is responsible for leading and managing all aspects of clinical research initiatives within the organization. Develop and implement strategic plans for clinical research programs in alignment with organizational goals and objectives. Oversee the design, development,...
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...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
Odyssey Systems Consulting Group, .We focus on people, processes, and performance to deliver superior results.Since our inception in 1997, our commitment to mission success and customer satisfaction has been recognized with exponential growth and exceptional past performance ratings.We accept challe...
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 ...
Excellentknowledge of Clinical Research methods andprocedures. Scor other diploma from a Clinical Researchprogram. Avalid Clinical Researchlicense. Yourexpertise and opinions shall be valuable to us which shall help usin ourresearch. ...
The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (CTOM...
The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. This role is responsible for completing case report forms (CRFs) and entering clinical...
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...
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...
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. ...
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...
Strong working knowledge of clinical operations and experience with clinical study conduct from start-up through close-out, with global trials or CRO management experience preferred. Candidates are expected to manage and oversee all study-level vendor and site related activities and issues related t...
Assist lawyers with writing and research for complex immigration filings. Duties include drafting supporting letters for national interest waiver, alien of extraordinary ability and outstanding researcher petitions. Requires Bachelor’s degree or higher degree in journalism, political science, philos...
Clinical Trial Manager / Senior Clinical Trial Manager. This role is a unique opportunity for an experienced Clinical Operations Professional with a background in Oncology and technical expertise in managing Phase I-III clinical trials in an industry setting and a strong knowledge of clinical operat...
Ensure audit-ready condition of clinical trial documentation including central clinical files; review monitoring visit reports to ensure quality and resolution of site-related issues; coordinates and assist in the planning of regulatory or ethics committee activities, as appropriate. Oversee the per...
As an Epic Implementation Third-Party Applications Project Manager with Ellit Groups, you will play a pivotal role in the successful implementation of third-party applications and integrations within the Epic EHR environment. Lead end-to-end project management for the implementation of third-party a...
Able to collect, analyze and present data to the research and management teams. ...