Coordinates with the Clinical Research RN to organize procurement of research samples and then prepares, packages and ships research samples. CLINICAL RESEARCH COORDINATOR II. Serve as primary contact with research participants, sponsors, and regulatory agencies. Collect and manage patient and labor...
A company is looking for a Market Research Coordinator to support their Streaming & Creator Platforms research team. Social Sciences, Psychology, Business, Marketing, Market Research, Statistics, Economics, or a related field preferredStrong organizational skills to manage multiple prioritiesAbility...
The Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. The Research Regulatory Coordinator also manages IRB-deferred studies, exempt and non-...
A company is looking for a Recruiting Coordinator, Market Research (Part-Time). ...
The Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. The Research Regulatory Coordinator also manages IRB-deferred studies, exempt and non-...
Research Coordinator, Clinical Research, Coordinator, Clinical, Healthcare, Education, Research. ...
The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the daily activities of a clinical trial and plays a critical role in the conduct of the study. Assists PI in development of materials and tools necessary to appropriately train individual...
The Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. The Research Regulatory Coordinator also manages IRB-deferred studies, exempt and non-...
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. Promotes the ethical conduct of research by actively participating in research related educational meetings/conferences (planning, presenting, etc. Promotes the ethical conduct of research an...
Ability to work effectively within a multidisciplinary team, including researchers, coordinators, and clinical staff. Coordinates & completes the day to day administrative & technical activities involved in a single complex, large, nationwide or multiple moderately complex concurrent biomedi...
Must have a minimum of 3 years of Clinical Research Coordinator experience working on a drug or device studies. Clinical Research Coordinator III. Manages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external...
Works in collaboration with Chief Integrity Officer and research leaders to develop and implement research compliance education and training programs for all research staff, including without limitation clinical research billing, research misconduct, human research protections, conflict of interest,...
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...
As a Clinical Research Coordinator, you will be at the forefront of managing daily operations of biomedical and/or social-behavioral research studies. Job Title: Clinical Research Coordinator. The team includes Clinical Research Managers, Project Managers, CRC Leads, CRCs, and Data Coordinators. You...
Will assist with the development of community Performs biomedical &/or social-behavioral research by administering tests &/or questionnaires following protocols. Conducts interviews and assessments of assigned patient population for clinical research evaluation. Assists with basic research a...
Understanding of the federal research regulations and the ability to identify the federal research organizations role in regulating human research participation. Identify and explain the responsibilities of Principal Investigators, research team members, sponsors, contract research organizations (CR...
Promotes the ethical conduct of research by actively participating in research related educational meetings/conferences (planning, presenting, etc. Based on specific research program needs, patient facing vs. Coordinates study conduct with other departments to effectively implement research projects...
The Pediatric Clinical Trials Office (Peds CTO) is an existing centralized support office that provides services and high-level guidance to individuals (faculty, investigators, research staff, and clinic coordinators from the University and Hospital) involved in human subjects research. The Pediatri...
Primary duties include: conducting literature searches and preparing literature tables; synthesizing information and preparing memos summarizing findings from scholarly publications in support of grant applications, presentations, and manuscripts; helping to prepare materials for research presentati...
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred. Assists clinical research personnel in the implementation of clinical research projects. High School Diploma with five to seven years clinical research experience -or- Associates/two years of...
EKG, blood collection)Processing all samples and shipping to Central LabMaintaining study sourceEntering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working ...
The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the daily activities of a clinical trial and plays a critical role in the conduct of the study. Strong organizational, writing, and speaking skills; able to collect, organize and maintain ...
Identifies and explains the responsibilities of Principal Investigators, research team members, sponsors, contract research organizations (CROs), and regulatory authorities related to the conduct of a clinical trial. Recruits and interviews potential study patients with guidance from PI and other cl...
The Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. The Research Regulatory Coordinator also manages IRB-deferred studies, exempt and non-...
Knowledge of research protocols, principles and procedures; knowledge of aspects of clinical trials such as screening, interviewing, case reports forms; knowledge of experimental design, mathematics, statistics, computer applications and computer data management; oral and written communication skill...