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
Senior Study Start-Up Specialist
A company is looking for a Contract Senior Study Start-Up Specialist responsible for overseeing and leading study start-up activities in collaboration with clinical research stakeholders. ...
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 ...
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 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 I
As a Clinical Research Associate focused on medical devices, you will play a crucial role in the planning, execution, and monitoring of clinical trials. Assist in the design and implementation of clinical study protocols, case report forms, and informed consent documents. Provide training and suppor...
Clinical Research Associate
The Clinical Research Associate will provide support to the Senior Director, Clinical Operations in managing and tracking key study deliverables and milestones. Assist with the review and development of study-specific protocols, CRFs, clinical study plans, manuals, tools, trackers and templates, etc...
Senior Clinical Research Associate - Rare Disease / Respiratory - West Coast
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 III (Clinical Research Coordinator)
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. Coordinate all aspects of the research protocol & ma...
Clinical Research Associate I -PER_DIEM, Schwab Lab
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...
Senior Clinical Research Associate
Job Title: Senior Clinical Research Associate. We are seeking a highly experienced Senior Clinical Research Associate (CRA) to join our dynamic team. The ideal candidate will have a strong background in clinical research, with a focus on monitoring and ensuring the integrity of our clinical trials. ...