Ascension Borgess HospitalN Neurosciences Institute Clinical Research, part of Ascension is looking for caring and compassionate Certified Nursing Assistants (CNAs) to join our team!. ...
Collects data and performs clinical assessment of research parameters. Certified Clinical Research Associate) or equivalent (SoCRA or. Coordinates research project in compliance with the. Provides education for patient and health care providers regarding various research protocols. ...
Two years of experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice. Facilitates, maintains, and coordinates the logistical aspects of assigned study protocols with other research staff in accordance with Good Clinic...
Clinical Research Coordinator III. Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols. Minimum of 5 years experience in Clinical Research. Adherence to ALCOA-C Standards with all the...
The Clinical Research Nurse (CRN) is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e. Certification by the ...
Duration: 12 Months (Possibility of extension) Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operat...
Responsible for efficient flow of clinical trial research including study feasibility, selection, start-up, conduct and close-out and for achieving performance targets on clinical trials to further establish Advocate Health as a premier research destination for patients and clinical trial sponsors. ...
The Clinical Research Director will lead, manage, and oversee the clinical research operations at a multispecialty outpatient medical clinic. The Clinical Research Director will collaborate with internal teams, external partners including Site Network Organizations, and patients to ensure the succes...
The Senior Clinical Research Coordinator (Sr CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). This position independently manages the collection, documentation, analysis of clinical trial data, and reporting of clinical res...
Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) or accredited institution. Field Clinical Research Assoicate. Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory...
The Clinical Research Nurse (CRN) is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (, investigator-initiated...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...
This position is entirely an on-site CRC role requiring daily travel to a primary site.This role may periodically require travel to a secondary site to provide support or temporary coverage as needed....
Two years of experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice. Facilitates, maintains, and coordinates the logistical aspects of assigned study protocols with other research staff in accordance with Good Clinic...
Two years of experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice. Facilitates, maintains, and coordinates the logistical aspects of assigned study protocols with other research staff in accordance with Good Clinic...
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
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 ...
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 Associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study protocols. ICON Strategic Solutions is currently hiring Clinical Research Associates for various clients (major pharmaceutical/ biotech companies) FSP ded...
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...
Entering 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 autonomously. Demonstrated ability to work independently, make informed decisions, and drive cli...
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 ...
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...
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...
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 ...