Are you a business? Hire clinical research associate candidates in Fort Lee, NJ
Montefiore Medical Center is seeking a Registered Nurse (RN) CCU - Coronary Care for a nursing job in Fort Lee, New Jersey. Job Description & Requirements Specialty: CCU - Coronary Care Discipline: RN Duration: Ongoing Shift: nights Employment Type: Staff The Montefiore RN maintains standards of ...
Montefiore Medical Center is seeking a Registered Nurse (RN) ED - Emergency Department for a nursing job in Fort Lee, New Jersey. Job Description & Requirements Specialty: ED - Emergency Department Discipline: RN Duration: Ongoing Shift: days Employment Type: Staff Provides professional nursing c...
Montefiore Medical Center is seeking a Registered Nurse (RN) ED - Emergency Department for a nursing job in Fort Lee, New Jersey. Job Description & Requirements Specialty: ED - Emergency Department Discipline: RN Duration: Ongoing Shift: evenings Employment Type: Staff This vacancy will be posted...
This is a full-time 12-month consultant/research associate (RA) position in Client's Pneumococcal Vaccine Global Access Strategy and Pricing (GASP) Team. Job Title: Research Associate (. Pneumococcal Access and Pricing Strategy Associate.
Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipm...
Upsilon Global are looking for an experienced Contract/Freelance Clinical Research Associate in the state of New York, to support several studies due to be held at the Memorial Sloan Kettering Cancer Center.
As a contract research organization (CRO) in pharmaceutical R&D and clinical studies, Panacro Pharmaceutical Technology Co.
Academic Scholar – Clinical or Research Assistant, Associate or Full Professor, Department of Pediatrics, Division of Neonatology.The Department of Pediatrics, University at Buffalo (UB), Jacobs School of Medicine and Biomedical Sciences and the Oishei Children’s Hospital are seeking candidates
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II assigned to Early Development trials (Phase I). ICON plc is a world-leading healthcare int...
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good Clinical Practice (GCP) and International Conference...
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 (C...
All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sex, sexual orientation, transgender status, gender dysphoria, national origin, age, religion, disability, military and veteran status, marital or...
Evaluate sponsor requirements and study team needs for novel technologies and lead execution and delivery of solutions with partnership across the MCIT teams including Architecture, Security and Clinical Applications. The Associate Director leads a growing team of individuals to support single-si...
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 g...
The Early Clinical Development Senior Clinical Research Associate will have relevant Phase I experience, responsible for conducting monitoring activities for one or more client sponsored studies. Responsible for monitoring clinical trial quality and site management for client sponsored studies th...
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nerv...
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have an ...
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management...
