A company is looking for a Study Start-Up Clinical Research Associate (SSU CRA) to manage site selection and activation phases of clinical trials.
Key ResponsibilitiesCollaborate with teams to identify and activate clinical trial sitesPrepare and manage regulatory submissions and start-up documentationTrack and manage essential documents to ensure timely site activationRequired QualificationsBachelor's degree in life sciences, nursing, or a related fieldAt least 2 years of experience in Site Selection Visits and Study Start-Up activitiesExperience with Informed Consent Forms (ICF) review is desiredKnowledge of ICH-GCP guidelines and local regulatory requirementsStrong organizational skills with a focus on timelines and deliverables
Study Start-Up Manager
A company is looking for a Manager, Study Start Up to manage site-level activities associated with clinical study start-up. ...
Clinical Research Associate
Under the supervision of the Clinical Operations Director, the Clinical Research Associate (CRA) is responsible for conducting all aspects of site monitoring for clinical research studies according to Phanes Standard Operating Procedures (SOPs) and ICH/GCP/GLP guidelines. Tracks and reports progress...
Clinical Research Associate
A company is looking for a Clinical Research Associate to support multiple projects in the healthcare field. ...
Assistant, Associate or Full Professor (Clinical X, In-Residence, Adjunct) Ophthalmology Research
The selected candidates will be responsible for the teaching and training of medical students, residents, and fellows in our educational programs as well as clinical research, translational research, and/or basic research. The Viterbi Family Department of Ophthalmology at UC San Diego (Department We...
Clinical Research Associate I -PER_DIEM, Department of Orthopaedics
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...
Clinical Research Associate
Job Title: Clinical Research Associate. Conducting pre-study, initiation, routine monitoring, and closeout visits. Training study investigators and staff. Tracking and reporting study progress. ...
Clinical Research Associate I, PER DIEM - Tan Lab
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...
Clinical Research Associate (CRA II/Senior) - West (Oncology)
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 ...
Senior Oncology Clinical Research Associate
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Develops site start up documents for studies including SIV agenda. Acts as Lead SM-training other SMs on study. Provides SM “voice” when reviewing study...
Clinical Research Associate
Conducts pre-study (site qualification) and routine monitoring to ensure visits are completed according to the Clinical Monitoring Plan(s) and SOPs. Ensures data collection timelines and deliverables are met at assigned clinical sites in accordance with study plans. Bachelor’s Degree (BA/BS) in life...