A company is looking for a Contract Clinical Research Associate (CRA).
A company is looking for a Contract Clinical Research Associate (CRA).
Clinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
read moreThe Clinical Research Associate,. This position will report to Vice President Clinical Development. Minimum 3 years of experience in clinical monitoring, late phase trials are a plus.
Clinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
read moreThe Clinical Research Associate,. This position will report to Vice President Clinical Development. Minimum 3 years of experience in clinical monitoring, late phase trials are a plus.
Responsible for coordination with clinical suppliers to ensure appropriate and timely delivery of clinical trial supplies to clinical sites. Tracking of clinical data, regulatory documents, and patien...
read moreTracking of clinical data, regulatory documents, and patient enrollment information and data resolutions to assure the timely completion of clinical studies in line with approved clinical development ...
read moreClinical Research Associateat Precision Medicine Group (View all jobs)Remote, United StatesPrecision for Medicine is not your typical CRO. Clinical Research Associate II/Sr. How you will spend your da...
read moreSeveral years of experience in the pharmaceutical industry with a focus on international clinical IMPs supply, as well as a good understanding of the clinical development processes. The DM Expert inde...
read moreClinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
read moreClinical Research Associate II/Sr. You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol,...
read moreSeveral years of experience in the pharmaceutical industry with a focus on international clinical IMPs supply, as well as a good understanding of the clinical development processes. The DM Expert inde...
read moreClinical Research Associate II/Sr. Clinical Research Associateat Precision Medicine Group (View all jobs)Remote, United StatesPrecision for Medicine is not your typical CRO. How you will spend your da...
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 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 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 moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreThe Senior Clinical Research Associate (CRA) will act as a liaison between BD (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. The Senior Clinical Research Assoc...
read moreResponsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to c...
read moreThe Senior Clinical Research Associate (CRA) will act as a liaison between BD (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. The Senior Clinical Research Assoc...
read moreClinical Research; 3 years of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is desired. The Clinical Research Associate is an integral part of ...
read moreClinical Research; 3 years of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is desired. The Clinical Research Associate is an integral part of ...
read moreIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. In depth knowledge of, and skill in ap...
read moreThe Clinical Research Associate will:. Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure ...
read moreInitiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and upda...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreWorldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...
read moreIQVIA 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 o...
read moreIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good knowledge of, and skill in applying, applicable clinic...
read moreGood knowledge of, and skill in applying, applicable clinical research regulatory requirements. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research ser...
read morePresent scientific results in internal research meetings.
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 indep...
read moreThe 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 indep...
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 moreClinical Research Associate (CRA) III. As a Clinical Research Associate (CRA) III, your responsibilities:. Strong knowledge of Good Clinical Practice (international quality standard for human clinical...
read moreThe 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 Healt...
read moreEmploy 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 (Electr...
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