Pediatric Neonatology Research -Clinical X Series, Associate or Professor Rank. The full-time academic appointment may be at the Associate, or Full Professor level in the Clinical X series, depending on experience and extent of research effort. See Professorial Series (Adjunct, Clinical X, HS Clinic...
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. The Clinical Research team conducts internal and external research studies and ensures t...
The CRA Manager is responsible for leading and managing a team of field-based Clinical Research Associates who monitor clinical trials at investigative sites. We are seeking a Clinical Research Associate (CRA) Manager to join our team at SpyGlass Pharma. This position ensures that clinical trials ar...
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. ...
We are seeking a Clinical Research Associate I (CRAI) who will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study. The Biomedical Imaging Research Institute (BIRI) is an interdisciplin...
As a Clinical Research Associate, you will play a crucial role in the planning, execution, and monitoring of medium and large-sized clinical trials. They are seeking a seasoned Clinical Research Associate to join their growing team. BS/BA in relevant discipline and at least 4 years of industry exper...
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 ...
Clinical research experience from a sponsor. Good computer skills in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file) preferred. We generate extensive clinical evidence to demonstrate the effectiveness and safety of ou...
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 ...
Strong knowledge of clinical research regulations (ICH-GCP, ISO 14155, FDA, and EU). Having received their series B not too long ago, they are making great strides in the product development for their minimally invasive product and they are looking for a clinical trial manager or senior CRA to aid t...
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 Clinical Research Associate will provide support to the Senior Director, Clinical Operations in managing and tracking key study deliverables and milestones. Minimum 5 years of experience directly supporting oncology clinical research trials in-house at a pharmaceutical company or CRO. This posit...
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. ...
Leads external scientific discussions and builds positive relationships with external physician partners * Leads or participates in monthly literature review with global teams; performs literature review as needed to support EGS and EDS * Handles budget associated with assigned r...
Job Title: Senior Clinical Research Associate. Bachelor’s degree in a relevant field or a nursing degree, with 4+ years of experience in clinical research, preferably in a sponsor company, CRA, or CRO setting. Collaborate with the Study Lead and project team to ensure the quality execution of clinic...
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. An advanced individual may conduct more complicated studies, as well as contribute to st...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
The Clinical Research Associate is responsible for clinical studies, site management and compliance monitoring of assigned clinical projects undertaken in support of a given product line or marketing initiative. Plan, implement and conclude clinical studies in support of project timelines/market rel...
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...
Lead Clinical Research Associate (CRA) reports to the Clinical Monitoring Manager responsible for site management oversight, with an emphasis on leading monitoring activities, training of CRAs and site staff, oversight of clinical CROs and supporting various study management and clinical quality (e....
I have an exciting part-time Clinical Research Associate role, on site based in Anaheim California!. Oversee the conduct of clinical trials at site, ensuring adherence to protocol, GCP, and regulatory requirements. Assist in the review and validation of clinical trial data to ensure accuracy, comple...