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...
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...
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...
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...
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 II, Career Outcomes & Assessment. In conjunction with a graduate coordinator, serves as the primary researcher in ...
Conceptually applies the research protocol to the clinical setting to allow accurate and timely completion of all duties. Provides a list of all study participants to facility/practice management to avoid improper billing of lab tests or services covered under the research budget. ...
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...
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. ...
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. ...
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 ...
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...
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. ...
Accepting applicants with either Clinical Experience, LPN (Licensed Professional Nurse), CMA (Certified Medical Assistant), Pharmacy Technicians or CRC (Clinical Research Coordinator). Barrington James is looking for Clinical Research Coordinators in multiple locations within Michigan to join our cl...
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...
Accepting applicants with either Clinical Experience, LPN (Licensed Professional Nurse), CMA (Certified Medical Assistant), Pharmacy Technicians or CRC (Clinical Research Coordinator). Barrington James is looking for Clinical Research Coordinators in multiple locations within Michigan to join our cl...
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...
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...
Prior experience in clinical research is not required but preferred. Medical Assistant Certification preferred. ...
Project Manager/Contractor Liaison - Manage project quality, budget and execution in a pharmaceutical setting by working with all members of the project team including process engineers, facilities, end users and contractors. Close coordination between construction activities/tasks and construction ...
In addition to a current License, individual must possess an MSW or MA from an accredited college or university in social work, rehabilitation counseling, or other related behavioral healthcare or counseling program. Program Director, Community Support Services (Supportive Housing). ...
Along with advising ICR's scientists about their own nutritional habits, our ideal candidate will also bring new, practical research ideas to the lab. Contribute practical research ideas to ICR bench scientists that may improve healthy aging. We're hiring an exceptionally talented PhD Nutrition Scie...
We are seeking an exceptionally talented scientist to serve as Associate Director for Scientific Programs. As an Associate Director with ICR, you'll get to:. Integrate and synthesize the latest research findings from multiple fields and contribute novel ideas to accelerate projects toward ICR’s ulti...