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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.
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. Under the direction of supervisor or designee, this position will ser...
Job Title: Research Associate (. This is a full-time 12-month consultant/research associate (RA) position in Client's Pneumococcal Vaccine Global Access Strategy and Pricing (GASP) Team. Pneumococcal Access and Pricing Strategy Associate.
Academic Scholar – Clinical or Research Assistant, Associate or Full Professor, Department of Pediatrics, Division of Neonatology. UB is a premier, research-intensive public university dedicated to academic excellence. Demonstrate excellent qualifications in education, clinical care or research. ...
As a contract research organization (CRO) in pharmaceutical R&D and clinical studies, Panacro Pharmaceutical Technology Co.
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...
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.
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.
Through the above mentioned partnership and an academic appointment at Rutgers, The State University of New Jersey, unique opportunities exist for collaborations between clinical and research programs, including clinical trials research, cancer chemoprevention, clinical and basic pharmacology, an...
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.
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...
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...
IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous System (CNS) or Cardiovascular/Renal/Metabolic (CVRM). IQVIA is a leading global provider of advanced analytics, technology solutions and...
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...
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...
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 ...
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
The Associate Director of Clinical Research will work with the MCIT leadership to be responsible for the implementation and operations of all aspects of clinical research systems for NYU Langone Health including product management, adoption, implementation, support, and operations. Employ product...
