Clinical research associate jobs in Kearny, NJCreate job alerts

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. Database analysis, primary market research, literature reviews, decision models, budget impact models, systema...

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.Consequently, we are seeking CRA's with a proven background within complexed Oncology and ...

Overseeing the management and administration of all aspects of clinical trials/studies involved in each step of the clinical study. As a contract research organization (CRO) in pharmaceutical R&D and clinical studies, Panacro Pharmaceutical Technology Co. Monitoring and coordinating the clinical ...

As a contract research organization (CRO) in pharmaceutical R&D and clinical studies, Panacro Pharmaceutical Technology Co. Overseeing the management and administration of all aspects of clinical trials/studies involved in each step of the clinical study. Monitoring and coordinating the clinical ...

The University at Buffalo (UB) is one of America’s leading public research universities and a flagship of the State University of New York system, recognized for our excellence and our impact. Demonstrate excellent qualifications in education, clinical care or research. Academic Scholar – Clinic

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. ICON plc is a world-leading healthcare intelligence and clinical research organization. C...

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...

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...

Assist with other assigned clinical responsibilities within scope of role to provide best practice and/or support to junior clinical staff. The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to ...

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 ...

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...

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.

As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

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...

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...

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...

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...

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 ...

Good Clinical Practice HIPAA and required obligations to the patient/subject Principle Investigator clinical research team and the sponsor The aCRC assists with general laboratory cleanliness and organization oversees and maintains a safe organized inventory system for the clinical trial kit supp...