Bachelor's degree in nursing, allied medical professions or other health care field required or equivalent combination of education and experience required; Current State of Ohio nursing license or other relevant board or interim permit required in appropriate field; clinical research certification ...
Desired skills include: Clinical research Dosage ranges Indications Ethical Research Principles & Practices Side effects Keen attention to detail Medical terminology Microsoft Office proficiency Licensing or Certifications for Clinical Research Nurse and Physician Assi...
Serves as Manager, CCRM Clinical Research Operations in the College of Medicine (COM) Center for Clinical Research Management (CCRM); participates in execution of activities in the CCRM Clinical Research Operations Office in collaboration with Directors-Clinical Research Operations; oversees multipl...
To provide assistance in support of clinical research studies within the Department of Anesthesiology/Spine Research Institute in collaboration with the College of Medicine Center for Clinical Research Management (CCRM); assists with implementation and coordination of studies; participates in recrui...
The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. Clinical Research Coordinator Certification (or equivalent approved Clinic...
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Department of Neurosurgery; assists with assessing patient records to identify patients who ...
MD) preferred10+ years of experience in oncology preferred, community-based preferred5+ years experience in clinical researchExperience building and leading successful oncology program development such as in clinical research, genetics, precision medicineAbility to travel up to 40%Anticipated salary...
Research and Scholarship Clinical Research Individual Contributor/Specialized S2. Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols. Assist with collecting, extracting, coding, and analyzing clinical research data. ...
Bachelor's degree in nursing, allied medical professions or other health care field required or equivalent combination of education and experience required; Current State of Ohio nursing license or other relevant board or interim permit required in appropriate field; clinical research certification ...
Clinical Research Assistant to provide support to assure research protocols are in compliance with university, state and federal regulations across research groups managed by the Clinical Trials Office (CTO); assists with regulatory functions in support of clinical research activity; assists in prep...
The Clinical Research Coordinator II is responsible for managing all of the elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. Conducts clinical studies as outlined in the study prot...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
The IGM Clinical Research coordinator’s primary responsibility is managing key elements of clinical research studies to meet protocol obligations. Conducts clinical research studies as outlined in the study protocol; discerns critical elements of the protocol to ensure subject safety throughout stud...
Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Clinical Research Coordinator III (RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work. KPA 1 Protocol Comprehension and Implementation: Coordination o...
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Division of General Internal Medicine's new Dissemination and Implementation Science (DIS) program within the Department of Internal Medicine; assists ...
The Clinical Research Nurse I (CRN) primary responsibility is managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. Performs research activities as outlined in the protocol; im...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
Desired skills include:Clinical research Dosage ranges Indications Ethical ResearchPrinciples & Practices Side effects Keen attention to detailMedical terminology Microsoft Office proficiency Licensing orCertifications for Clinical Research Nurse and Physician AssistantList any licenses or certifica...
The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requi...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Clinical Research Coordinator, Comprehensive Cancer Center, Clinical Trials Office. Research and Scholarship – Clinical Research – Individual Contributor/Specialized – S2. The Clinical Research Coordinator. Assist with assessing patient records to identify patients who are eligible to participate in...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Clinical Research Associate II (CRA II) - Position Title: Clinical Research Associate Function: Clinical Service Overview: This individual will be responsible for managing clinical activities at study sites conducting studies for the Medical Devices group, as well as, fostering strong, productive re...