Coordinates with the Clinical Research RN to organize procurement of research samples and then prepares, packages and ships research samples. CLINICAL RESEARCH COORDINATOR II. Collect and manage patient and laboratory data for clinical research projects. Collect and manage patient and laboratory dat...
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....
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...
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. ...
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...
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...
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...
The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (CTOM...
Month Contract Clinical Research Coordinator role in Oak Park, IL (60302). We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team and assist with vaccine trials. The ideal candidate will play a critical role in coordinating and overseeing the daily activities 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...
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 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 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...
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. ...
Assisting Clinical Research Coordinators or other staff members as determined by the needs and priorities of the research organization, and as time and abilities permit. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. Per...
Bonus: previous experience in clinical research. Provides administrative and clinical support, including taking vital signs and assisting with participant visits, as needed. Adhere to Good Clinical Practices. Supports clinical and administrative team. ...
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...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion. Abili...
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...
The Clinical Research Coordinator is an essential team member in the conduct of dietary, exercise and pharmaceutical studies. This position acts as a point person for the clinical-study site, overseeing all operational responsibilities for the successful launch, enrollment, maintenance and completio...
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...
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 ...