SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies f...
Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within rep...
Serves as primary study coordinator ensuring adherence to the research protocol and provides periodic updates to Principal Investigator on study progress. Collaborates with the research nurse coordinator in creating source documents. Screens research subject /participants as delineated in study spec...
The Clinical Research Coordinator III will serve as a member of the Clinical Research team. Rutgers, The State University of New Jersey is seeking a Clinical Research Coordinator III (CRC III) for the Department of Medicine-Infectious Diseases within the New Jersey Medical School. This position is r...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Coordinator will conduct study operations and activities of designated studies, including those that are part of the ...
Clinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulations. ...
Clinical Research Coordinator III A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Occasionally attending out-of-town Investig...
Required Skills: Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management. Join us and help clients adapt to evolving requirements in ...
Rutgers The State University of New Jersey is seeking a motivated Temporary Research Coordinator for the Department of Pediatrics at Rutgers Biomedical and Health Sciences. The primary purpose of the Temporary Research Coordinator will be to work mostly at the CRC at the Child Health Institute and t...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Coordinator will conduct study operations and activities of designated studies, including those that are part of the ...
Rutgers University- Newark (RU-N), an urban public research university and anchor institution, located in Newark, New Jersey, a city of promise is seeking a Research Project Coordinator I, Career Outcomes & Assessment. In conjunction with a graduate coordinator, serves as the primary researcher in t...
The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including, but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human...
Job Description: Studies Coordinator – Photoprotection. We are looking for a detail-oriented and proactive Studies Coordinator to join our Photoprotection – US Clinical & Instrumental Evaluation Intelligence Team. Contact Contract Research Organizations (CROs) to coordinate testing timelines, manage...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies f...
As the leading academic health system in New Jersey, we advance innovative strategies in high-quality patient care, education, and research to address both the clinical and social determinants of health. ...
The Research Coordinator coordinates and performs all the associated duties associated with coordination and implementation of the conduct of clinical research trials and projects. A day in the life of a Research Coordinator at Hackensack Meridian Health includes:. Serves as primary study coordinato...
The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including, but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human...
Those aren't words that are usually associated with a job. For Associate Director level with Ph. Research Investigator, with Ph. For Research Investigator, with Ph. ...
The RN Clinical Care Coordinator will be the primary care manager for a panel of members with complex medical/behavioral needs. BSN, Master's Degree or higher in clinical field. ...
Budgeting, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Financial Analysis, Health Sciences, Life Science. We have an opportunity for a Senior Clinical Research Associa...
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The purpose of this role is to implement the Alzheimer's Association's program delivery and growth strategy to reach more people with volunteer-delivered programs, especially in new, underrepresented and rural communities. The Coordinator is responsible for identifying, recruiting, engaging and grow...
The Research Assistant will assist the PI in researchactivities such as programming and performing psychophysical experiments, operatingeye-tracking equipment, testing models, carrying out data analysis, andcontributing to journal publications, conference submissions, and grantapplications. Research...
Budgeting, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Financial Analysis, Health Sciences, Life Science. Excellent knowledge of the drug development process specifica...
The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. The CP&P team interacts with discovery and translational scientists, project leadership, earl...