The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...
read moreEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
read moreThe Clinical Pharmacy Specialist (CPS) is the designated hospital-wide expert in the area of clinical pharmacy and directly provides leadership for the continued growth of comprehensive clinical pharm...
read moreThe Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...
read moreResponsible for providing Clinical Research support for all clinical trials. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible f...
read moreResponsible for providing Clinical Research support for all clinical trials. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible f...
read moreWhen required, serve as a principal level Statistical Programmer, working effectively with interdisciplinary teams to contribute strategically (through innovative ideas or applications) to drug develo...
read moreThe Clinical Research Associate I monitors all aspects of clinical research trial(s) Clinical study life-cycle responsibilities including site management, ongoing maintenance and closure of pre-clinic...
read moreThe Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials. Under the direction of the Clinical Study Manager(s)...
read moreResponsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Generate cl...
read moreResponsible for providing Clinical Research support for all clinical trials. Participate in the evaluation of potential clinical sites according to established criteria of acceptability. Responsible f...
read moreThrough 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...
read moreMaintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities. At least 4 years' ex...
read moreDuties and Responsibilities Act as the primary point of contact with assigned clinical study sites during start-up activities; Working with finance and legal experts, drive contract and bu...
read moreMaintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities. At least 4 years' ex...
read morePerform a key role in building relationships with site Clinical Coordinators, Study Investigators, and Service Provider partners and contribute significantly to the execution of the clinical trial. BS...
read morePerform a key role in building relationships with site Clinical Coordinators, Study Investigators, and Service Provider partners and contribute significantly to the execution of the clinical trial. Sy...
read moreThe Clinical Pharmacy Specialist (CPS) is the designated hospital-wide expert in the area of clinical pharmacy and directly provides leadership for the continued growth of comprehensive clinical pharm...
read moreThe Clinical Pharmacy Specialist (CPS) is the designated hospital-wide expert in the area of clinical pharmacy and directly provides leadership for the continued growth of comprehensive clinical pharm...
read moreAs a Clinical Research Associate, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. Other interfaces include Study Responsible ...
read moreMaintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities. At least 2 years' ex...
read moreMaintain current knowledge related to cancer therapy, clinical trial design and conduct, and good clinical practice through literature reviews and other educational opportunities. At least 2 years' ex...
read moreThe 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. Focused primarily on ensuring...
read moreThe 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. Good Clinical Practices (GCP)...
read moreInnova Solutions has a client that is immediately hiring for a.Position type: Full-time, contact.Location: New Brunswick, NJ (50% onsite).
Innova Solutions has a client that is immediately hiring for a.Position type: Full-time, contact.Location: New Brunswick, NJ (50% onsite).
Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intell...
read moreGood Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intell...
read moreAdvanced knowledge of Clinical investigation of medical devices for human subjects - Good Clinical Practice (ISO 14155), 21 CFR Part 11, 50, 54, 812 and other applicable regulations, fundamental knowl...
read moreEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
read moreEverest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechn...
read moreGood Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research servic...
read moreIQVIA 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/Met...
read moreGood Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management according to executed clinical trial agreem...
read moreCulture primary cells and continuous cell lines such as neutrophils, hematopoietic stem cells, immune cells, and/or relevant cell lines to support in vitro/ex vivo experiments.Perform in vitro assays ...
read moreCulture primary cells and continuous cell lines such as neutrophils, hematopoietic stem cells, immune cells, and/or relevant cell lines to support in vitro/ex vivo experiments.Perform in vitro assays ...
read moreThe Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice.
This position serves as a key role in the effective implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds ...
read moreThis position serves as a key role in the effective implementation of the global development strategy leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds ...
read moreAs an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related...
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