The Associate Research Scholar / Clinical Fellow will hold the University title of Associate Research Scholar. Columbia Law School seeks an experienced lawyer with a background in criminal defense and...
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 moreThe Associate Research Scholar / Clinical Fellow will hold the University title of Associate Research Scholar. Columbia Law School seeks an experienced lawyer with a background in criminal defense and...
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.
Tracking 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 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 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. 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 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. 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 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 moreWorks 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 co...
read moreKelly® Science & Clinical is seeking a Clinical Research Regulatory Affairs Associate for temporary, temporary-to-hire, and direct hire positions at a leading client in Philadelphia, PA. Our clie...
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 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 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 moreAt least three (3) years of relevant and complex clinical research experience Preferred. Intermediate knowledge of clinical research methods. This role supports the work of Lisa Eidenschink Brodersen,...
read moreAs 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 T...
read moreAs 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 T...
read moreWe’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 Associ...
read moreWe’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 Associ...
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 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 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. If applicable, may be accountable for site financial manage...
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 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 moreUnique opportunities exist for collaborations between clinical and research programs, including clinical trials research, cancer chemoprevention, clinical and basic pharmacology, and Phase 1 clinical ...
read moreUnique opportunities exist for collaborations between clinical and research programs, including clinical trials research, cancer chemoprevention, clinical and basic pharmacology, and Phase 1 clinical ...
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 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...
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