Good Clinical Practice, GCP, IRB, international review board, FDA, pharmacology, toxicology, biochemistry, biology, chemistry, immunology, clinical trials, ICH, regulatory documents, data management, tmf, trial master file, standard operating procedures, protocols, adherence, sop, IND, Investigation...
Work collaboratively with Clinical Trials Operations and Biostatistics (CTOBB) staff, Principal Investigators (PIs), Clinical Coordinators, Government Project Officers (GPOs) and Institute Contracting Officers; advise CTOBB regarding the findings of on-site observation of activities of both the Clin...
The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applica...
Certified clinical researcher with one of the following accredited organizations: Association of Clinical Research Professionals Certified Professional (ACRP-CP); Association of Clinical Research Professionals (ACRP); Certified Clinical Research Professional (CCRP); Certified Clinical Research Coord...
Minimum of four (4) years of experience in a clinical research environment. NICHD’s mission is to lead research and training to understand human development, improve reproductive health, enhance the lives of children and adolescents, and optimize abilities for all. Communicate abnormal results and p...
Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP). Clinical Trials Research Nurse Manager. You will be assisting with the development, implementation, and evaluation of clinical trials for research by pharmaceutical companies, device manufacture...
University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research. Proven knowledge of project management tools and processes Proven experience in clinical development/drug development process in various phases of development and therapy ...
The Associate Director, Business Development Clinical Research US will focus on building new and maintaining productive client relationships in the clinical research industry for the SGS Clinical Research Services. They will be able to achieve individual and team revenue and sales objectives through...
Clinical research, Late phase, Clinical Operations, clinical development, Clinical projects. On behalf of the Senior Global Clinical Operations Program Director (Sr GPD), the GPD provides strategic operational leadership and oversight of a suite of globalclinical studies within a program covering al...
These support services include dedicated clinical research professionals who provide patient care to clinical trial participants at the National Institutes of Health (NIH) Clinical Center, and other research services that support the domestic and international clinical research initiatives of the Na...
Our healthcare organization is looking for a Clinical Research RN to work directly with physicians executing clinical research projects in an acute care/inpatient setting. Oversees clinical research studies, collecting all clinical data in an accurate and timely manner. Coordinates critical research...
University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research. Proven knowledge of project management tools and processes Proven experience in clinical development/drug development process in various phases of development and therapy ...
Lead in the design, development and testing of electronic clinical quality measures using Clinical Quality Language (CQL), Quality Data Model (QDM) and Fast Healthcare Interoperable Resources (FHIR). Provide strategic and technical expertise related to digital quality health and clinical informatics...
Performing routine and for-cause monitoring of human subjects research and protocols that received research determinations to ensure the appropriate regulations were applied during the review of the study and ensuring the research/activity is conducted as approved. Knowledge and experience in the ar...
Clinical Research Advisor to work onsite with the National Institutes of Health in Rockville, MD. Formulates guiding principles and Standard Operating Procedures (SOPs), and prepares staff for clinical research. Certified Clinical Research Associate (CCRA). Minimum of nine (9) years of experience co...
Performs a variety of complex duties to support the conduct of clinical research, such as, facilitating the informed consent process, coordinating required research activities; collecting, compiling, and documenting clinical research data to ensure adherence to protocols and validation of informatio...
HJF's support and administrative capabilities allow military medical researchers and clinicians to maintain their scientific focus and accomplish their research goals. Clinical Research Coordinator II. This position will be in support of Infectious Disease Clinical Research Program (IDCRP) located a...
The Principal Investigator will be responsible for a variety of specialized clinical research activities, ensuring that established protocols are implemented, maintaining protocol integrity, monitoring participants' status and safety, and playing a significant role in the education of clinical staff...
Work collaboratively with Clinical Trials Operations and Biostatistics (CTOBB) staff, Principal Investigators (PIs), Clinical Coordinators, Government Project Officers (GPOs) and Institute Contracting Officers; advise CTOBB regarding the findings of on-site observation of activities of both the Clin...
Good Clinical Practice, GCP, IRB, international review board, FDA, pharmacology, toxicology, biochemistry, biology, chemistry, immunology, clinical trials, ICH, regulatory documents, data management, tmf, trial master file, standard operating procedures, protocols, adherence, sop, IND, Investigation...
A BSN or BA or BS in psychology, nutrition or a related field with at least 1 year of experience conducting human subjects research, clinical trial/clinical research experience or an equivalent combination of education and experience are desired. The Coordinator will conduct semi-structured clinical...
Assist in resolving compliance issues at clinical sites, clinical vendors, and contracted research facilities, provide assessment of the impact of any deficiencies, and identify ways to standardized processes to improve quality and/or facilitate efficiency. Minimum of five (5) years of experience in...
All applicants must have experience or interest in hypertension research or cardiovascular health research, clinical trials, and health equity research. Postdoctoral Position in Hypertension, Blood Pressure Measurement, Clinical Trials and Community Based Research. The primary responsibility of the ...
These support services include dedicated clinical research professionals who provide patient care to clinical trial participants at the National Institutes of Health (NIH) Clinical Center, and other research services that support the domestic and international clinical research initiatives of the Na...
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 mini...