Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. Responsible for managing the research activities at sites participating in Worldwide’s clinical...
Join Kelly FSP as a Regional Clinical Research Associate fully dedicated to a Medical Device organization!. ...
Reporting to the Lead Clinical Research Associate, the CRA II/Sr. This role will collaborate closely with key cross-functional internal stakeholders including Clinical Operations, Medical Monitoring, Data Management, Supply Chain, and Clinical Compliance and Quality as well as external CRO and vendo...
We are seeking an experienced Senior Clinical Research Associate to oversee and manage clinical trials for our client in the peripheral vascular device space. The ideal candidate will have a strong background in clinical research, with specific expertise in vascular medical devices. Manage all aspec...
Clinical Research Associate (Part-Time). Collaborate with Contract Research Organizations (CROs) and vendors to ensure efficient delivery of study materials and documentation to investigator sites. Minimum of 2+ years of clinical monitoring experience in oncology trials required. ...
The Senior Clinical Research Associate will report to Manager, Clinical Affairs, and will play a key role to proactively support the conduct of pre-market and post-market clinical studies to ensure compliance with all the regulatory requirements. Contribute to all clinical research activities to ens...
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 Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
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...
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 ...
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...
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 ...
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. ...
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. ...
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 Assistant Coordinator-Oncology Research serves as regulatory assistant and administrative support for the Oncology Clinical Research department in order to facilitate the implementation and management of oncology clinical trials, assists in document preparation and maintenance for study mandated...
The Research Assistant supports the execution of certain aspects of a research project after the research design is established with minimal supervision. Able to read; write legibly; speak in English with professional quality; use computer, printer, and software programs necessary to the position; A...
The Coordinator-Admin Research is responsible for coordinating and facilitating research in the department and includes activities undertaken by attending physicians, residents, and medical students. This position will also be responsible for overseeing research cost with department administration a...
Coordinator-Clinical Research 3 is responsible and accountable to oversee and coordinate the implementation and management of research trials. Certified Clinical Research Coordinator (SoCRA, ACRP) required within six months of hire date required. Our mission is to participate in Jesus Christ's minis...
The Senior Research Assistant assists in entering and maintaining all documentation and records. Minimum two years of administrative/clerical experience required; one year research or laboratory experience preferred. Completion of LLU's educational program on "ethical use of human subjects in resear...
The Associate Project Coordinator effectively coordinates and communicates with our customers, field sales representatives, sales support, production, purchasing, shipping and inside sales on tasks needed to support sales on primarily multi-family and commercial projects. As an Associate Project Coo...
Manage projects and documents from start to finish including: cost requests, change orders, draws, project schedule, project submissions, subcontracts and owner contracts. Years in estimating and/or project management. ...
The successful Project Manager will have solid IT project management experience in a software engineering and/or information technology field, excellent written and verbal communications skills in English and experience leading cross-cultural, remote and global project teams and customers. Canonical...
Assist Project Manager in tracking Project Blueprint, Build, Test, cutover activities by assisting in update/ sync of Project artifacts using Box, Smartsheet, Jira, etc. Provide support to ensure projects have required documents in order to mobilize projects. IT Applications project execution coordi...
The IT Project Manager will be responsible for managing assigned resources, creating and tracking detailed project plans, effectively leading and facilitating project meetings, as well as proactively controlling project scope, risks and issues. As the IT Project Manager, you will be part of the Proj...