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
Oncology Clinical Research Associate
A company is looking for a Clinical Research Associate - Oncology. ...
Clinical Research Associate II - Obstetrics & Gynecology - Minimally Invasive Gynecologic Surgery (Full-Time, Hybrid)
The Clinical Research Associate II works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors. Provides limited patient cont...
Clinical Research Associate
A company is looking for a Clinical Research Associate to support multiple projects in the healthcare field. ...
Senior Clinical Research Associate - West Coast
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...
Study Start Up Specialist
A company is looking for a Study Start Up/Feasibility Specialist to manage the start-up phase of clinical trials. ...
Associate Clinical Research III
The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. Responsible for ensuring shipment of study devices and supplies to clinical sites and performing study device accountability. Solid understanding and demonstrated exp...
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
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 ...
Staff Research Associate II (Clinical Research Coordinator)
May be responsible for the coordination of one or more clinical studies or clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding participants; may apply understandin...
Staff Research Associate IV (Clinical Research Coordinator)
The CRC will be responsible for the coordination of one or more clinical studies or clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical, surgical and laboratory data regarding participants; apply underst...