Experience in a clinical research capacity conducting clinical research trials preferred;. SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals). Patients that are enrolled and participating in clinical research studies/trials. The RN-PCC coordinate...
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...
Senior Clinical Research Coordinator serves as lead resource in the execution of assigned basic science clinical research studies in accordance with approved protocols by scientists in the School of Health and Rehabilitation Sciences; oversees, implements amp; coordinates conduct of daily activities...
Experience in a clinical research capacity conducting clinical research trials preferred; and/or experience in nursing required with experience in specialty area nursing preferred; certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Profession...
To provide assistance in support of clinical research studies within the College of Medicine Department of Obstetrics and Gynecology/ Maternal Fetal Medicine; assists with implementation and coordination of studies; participates in recruitment of study participants; performs behavioral or diagnostic...
Experience in a clinical research capacity conducting clinical research trials preferred; and/or experience in nursing required with experience in specialty area nursing preferred; certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Profession...
The Clinical Research Coordinator II’s primary responsibility is 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. Performs research activities as outlined in th...
Job Title:Physician - Plastic Surgery - Vice Chair of Clinical Research. Job Summary: The Physician provides licensed medical care including diagnosis, treatment (inclusive of surgery or pre/post-surgical care where appropriate), case management and clinical research. The Physician must be competent...
Summary:The Senior 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 ...
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. ...
Responsible for all aspects of clinical compliance and data quality for cancer treatment protocols within assigned research bases. Maintains a thorough knowledge of assigned protocols and adheres to research principles and guidelines for meeting time lines and data management requirements. ...
Primary responsibilities of this position include: 1) recruitment of research participants 2) collection of qualitative and quantitative research data; 3) preparing IRB protocols; 4) maintain compliance with IRB and study training and documentation requirements; 5) management, tracking, and limited ...
The Director will lead toxicologists and clinical research for the overall safety assessments from raw material to finished product, and preparation of cosmetic safety report, responsible for post market surveillance and cosmetic adverse event monitoring, analyzing and reporting as required by cosme...
A bachelor's degree in a healthcare or health science field or nursing required; two years experience in clinical research or knowledge of clinical research required; data collection, data entry, and data reporting experience required; knowledge of medical terminology required; computer skills, expe...
Field monitor 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 moni...
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. ...
The Clinical Research Coordinator I is responsible for managing elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. Skills:Understanding of medical terminology and clinical research p...
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 ...
Senior Clinical Research Coordinator serves as lead resource in the execution of assigned basic science clinical research studies in accordance with approved protocols by scientists in the School of Health and Rehabilitation Sciences; oversees, implements & coordinates conduct of daily activities of...
The Consultant, Research & Clinical Development QA, Nonclinical Quality will be responsible for providing assistance to the Quality Assurance Unit in their GLP oversight of the general Quality Systems and nonclinical studies conducted at Sarepta, OH GTCOE site. This position will report to the Direc...
To provide assistance in support of clinical research studies within the Department of Internal Medicine/Division of Endocrinology in partnership with the College of Medicine Center for Clinical Research Management; assists with implementation and coordination of studies; participates in recruitment...
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...
Clinical Research Assistant, Comprehensive Cancer Center, Clinical Trials Office. Research and Scholarship – Clinical Research – Technical – T2. Experience with human subjects training in a clinical research capacity or setting desired. Experience in a clinical and/or research setting working with p...
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...
Summary: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 approve...