Our Fortune 500 global Pharmaceuticalclient is seeking an experienced Delivery Lead Associate, Clinical TrialPatient Engagement. Job Summary: The Delivery Lead (DL) is responsible for supporting the design strategy for patient recruitment & retention within our clinical
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Grants and Contracts Associate - SPH Office of Research Services Hiring Department: School of Public Health Office of Research Services Location: Chicago, IL USA Requisition ID: 1042838 FTE: 1 Work Schedule: Monday - Friday, 9:00AM - 5:00PM
Job Posting Title:Contract Officer or Senior Contract Officer, Office of Sponsored Projects - Hiring Department:Office of Sponsored Projects - Position Open To:All Applicants - Weekly Scheduled Hours:40 - FLSA Status:To Be Determined at Offer - Earliest Start Date:Ongoing
Grants And Contracts Manager (Remote) Lead a team of Administrators to support complex grants and contracts that drive impactful research and meaningful outcomes. Be You. This position will be located within the School of Medicine Shared Research Administration
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and
Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work
Please submit your application in English What Youll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document
Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all
Fortreas FSP team is hiring a Clinical Operations Manager- Regulatory - Hybrid in Montreal, Canada. Must be bilingual in French & English. Candidates with strong organizational skills, attention to details, and the ability to manage financial
ABOUT VITALIEF Vitalief is a clinical research consulting firm focused exclusively on the clinical research industry, providing consulting, staffing, and technology-enabled services to academic medical centers, health systems, sponsors, CROs, and site networks. By combining deep
Role Summary The clinician contributes towards providing medical and scientific expertise and oversight for Clinical Trials conducted worldwide with a primary focus in Japan and the Asia-Pacific region. The clinician may be required to design a
Location:Zangmeister Cancer Center Pay Range:$26.54 - $49.29 Job Description Summary Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator III (RN) performs tasks independently, consistently and
Job Description Sr. Manager, Clinical Management, (Early Phase: Immunology/Auto-immune) Job Summary Under the direction of the Director/Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the oversight and management of Otsuka EARLY
Job Overview: Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
Job Overview: Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
Precision for Medicine is a Clinical Research Organization. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and
Locations: London, United Kingdom Categories: Site Activation & Maintenance Req ID: 12971 We are seeking a key manager to support the Medpace Study Start-up group in Europe while being office-based in London. This position will be
Role Summary Responsibilities: You will work on a range of projects involving the set-up and management of de novo, global real-world evidence (RWE) studies, including ethics applications and site support Salary: $95,000 - $105,000 per annum,