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...
Successful candidates would be expected to participate in the clinical, educational, and research activities of the Center for Cognitive and Memory Disorders, a multidisciplinary group with behavioral neurologists, neuropsychiatrists, research scientists, neuropsychologists, psychometrists, social w...
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...
Provides assistance in support of clinical research studies being conducted in the Department of Emergency Medicine; participates in the recruitment of study participants; collects and provides relevant data to be used in assessing eligibility of patients for participation in protocols; assists with...
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...
The Clinical Research Nurse is an integral member of the Pulmonary Transitions Program team at the OSU East Hospital. The Clinical Research Nurse will identify suitable patients to benefit from this program and facilitate transitional care starting just prior to hospital discharge. The Clinical Rese...
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 ...
Bachelors Degree in biological sciences, health sciences or medical field or an equivalent combination of education and experience required; three to five years experience in a clinical research capacity conducting clinical research studies required; experience in a progressively responsible managem...
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...
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 ...
We are seeking a full-time Clinical Research Coordinator to join Principal Investigator Dr Sarah O’Brien’s research laboratory. Dr O’Brien’s research focuses on the intersections between women’s health and hematology and seeks to improve recognition of bleeding disorders in women. Performing researc...
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. ...
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 ...
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...
Clinical Research Senior Coordinator serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the oversees, implements & coordinates conduct of daily activities of research studies; recruits, interviews and promotes study to...
Senior Clinical Research Associate positions open for a Biotechnology client. The ideal CRA will monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating p...
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 ...
Serves as the contact for physicians, nurses and other ancillary hospital staff to assure that all research and related clinical needs are achieved. Maintains accurate awareness of all clinical projects within the research center. YEARS OF EXPERIENCE: 3-5 years critical care experience required with...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and...
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...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
YEARS OF EXPERIENCE: 2-4 years clinical research experience with conducting clinical trials/studies. Preferred clinical research certifications, such as CCRA or other applicable research certifications. Specialized research professional working with and under the direction of the Principal Investiga...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
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...