Are you a business? Hire clinical research associate candidates in Englewood, NJ
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 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...
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 a m...
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...
The aCRC supports the management of the research biospecimen/biofluid components of clinical research studies, performs accurate execution of research protocols in accordance with PCC CTO Research Biofluids Management Unit (RBMU) standard operating procedures, Good Clinical Practice, HIPAA and re...
The Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate can function independently and is the lead Research Associate for the disease group which includes mentoring, train...
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...
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. CRA functions as a member of the clinical study team and performs study monitoring according to Good ...
Employ product management mindset in order to ensure the successful delivery of Clinical Research products such as Clinical Research Management Systems, Clinical Trials Management Systems, EDC (Electronic Data Capturing), eConsent, Regulatory eBinders, etc. The Associate Director of Clinical Rese...
Senior Clinical Research Associate. 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.
Whatunites and motivates our global team is the inspiration of our commonpurpose:To innovate for healthcare,building on our remarkable legacy of pioneering ideas that translate into evenbetter healthcare products and services. Do you wantto join us in helping to fight the world’s most threatening...
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. ICON plc is a world-leading healthcare intelligence and clinical research organization. W...
The Senior Clinical Research Associate (CRA) will act as a liaison between Ferring (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Ensure site(s) maintains an acceptable inventory of clinical supplies and associated documentation. Understanding of domestic ...
Maintain basic knowledge of research study design and clinical research specimen collection procedures associated with clinical trials Understands the principles of most research tests performed in research clinical trials. Good Clinical Practice HIPAA and required obligations to the patient/subj...
Request: Clinical-Scientific - Research Associate. Job Description: This is a full-time -month consultant/research associate (RA) position in Client's Pneumococcal Vaccine Global Access Strategy and Pricing (GASP) Team. Basic competence with methodological approaches and tools in health services ...
A masters or PhD degree is required in one of the following: epidemiology, biostatistics, health services research, health policy, public health, health economics, economics, or equivalent graduate degree. Basic competence with methodological approaches and tools in health services research is re...
... Research Associate covering Biotechnology. The responsibilities include assisting the Senior ... D., PharmD., or equivalent) and 2-5 years industry, clinical, and/or consulting experience; Strong ...
Staff The Patient Care Coordinator participates in performance improvement/research activities ... We are committed to recruiting and creating an environment in which associates feel empowered to ...
Associate's Degree in Nursing (ADN) minimum required. Bachelor of Science in Nursing (BSN ... Research and teaching skills * Change management and demonstrated problem-solving skills
