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. ...
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 doc. ...
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...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
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. ...
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 ...
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...
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...
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...
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...
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 ...
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 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...
A global role reporting into Senior Manager, Clinical Research Pharmacy Services supporting IP Management specific deliverables in Clinical Trial Execution. Broad work experience in life sciences or medically related field, including biopharmaceutical clinical research experience working on clinical...
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...
Minimum of 3-5 years of clinically-related experience, of which 3 years must be in clinical research monitoring. The Regional Clinical Research Associate provides site qualification, initiation, remote and interim monitoring, and study closeout visits. Bachelor’s Degree, preferably in a clinical sci...