Clinical Research Coordinator
Opening : Clinical Research Coordinator
Contract : 6 month Contract to Hire
Location : Onsite (Phoenix AZ).
Hard Requirements :
- Investigator Initiated Trial experience
- Being able to interpret protocol and ensure that it its done correctly.
- 3-5 years experience minimum with clinical trials.
Responsibilities :
- Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability.
- Provides study specific, individualized education to study subjects and families. 1.3 Ensures all appropriate subject consents are obtained.
1.4 Collects and processes protocol required specimens.
- Acts as a liaison between Sponsor, Investigator, and Study Subject
- Collects all required study data and completes CRFs in a timely, accurate manner.
- Ensures study documents are maintained in compliance with applicable regulations, guidelines, and policies (i.e. FDA, OHRP, IRB)
- Collaborates with Investigator to identify adverse events / serious adverse events to ensure study subject safety and accurate and timely reporting.
- Ensures appropriate internal and external customer service by demonstrating professional interactions with Sponsor, study monitors, and other departments.
- Complies with all regulatory and policy requirements.
- Demonstrates knowledge of federal and state regulations, guidelines, and policies governing the conduct of clinical trials.
Clinical Research Coordinator Idaho State Licensed
A company is looking for a Clinical Research Coordinator. ...
Clinical Research Coordinator II Neuroscience
Responsibilities Job Summary The Research Data Coordinator II is the primary contact with the study sponsor and is responsible for the day-to-day management of project activities and resources and overall clinical data and protocol management for the conduct of therapeutic clinical trials at HonorHe...
Clinical Research Coordinator
As a Clinical Research Coordinator, you’ll oversee and facilitate the clinical research activities. Supports the safety of clinical research procedures, study visits, and follow-up care. At least 1 year clinical research experience to include consenting patients. Ability to adhere to Good Clinical P...
Clinical Research Coordinator I, Internal Medicine (Multiple Positions) College of Medicine -Phoenix
The Department of Internal Medicine at The University of Arizona College of Medicine –Phoenix, is hiring multiple clinical research coordinators to support the RECOVER study and other COVID-19 related research studies. Clinical Research Coordinator I, Internal Medicine (Multiple Positions) College o...
Clinical Research Coordinator
Possession of Clinical Research Coordinator Certification (CRCC). Provides study information and obtains relevant information to and from patients engaged in clinical studies, which includes: assisting in the recruitment and screening of volunteers; registering patients; providing information on cli...
Clinical Research Coordinator
Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), and institutional guidelines, which includes the following duties: Reviews all regulatory requirements to ensure implementati...
Clinical Research Coordinator FT Days
The Clinical Research Nurse ensures that all study activity is in accordance with standard operating procedures, good clinical practice and instructions/specifications outlined in the research protocol. Clinical Research Coordinator Full Time Days Position Summary. The primary responsibility of the ...
Clinical Research Coordinator II Neuroscience
The Research Data Coordinator II is the primary contact with the study sponsor and is responsible for the day-to-day management of project activities and resources and overall clinical data and protocol management for the conduct of therapeutic clinical trials at HonorHealth. The comprehensive netwo...
Research Coordinator - Clinical
We are looking for a qualified and experienced Research Coordinator. Manages and coordinates all aspects of conducting clinical trials within Ironwood Physicians, PC facilities, both clinically and administrative/regulatory. Reviews studies for clinical and operational feasibility, along with the In...
Clinical Research Coordinator, On-Site
Clinical Research Coordinator experience within a similar setting. This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. IQVIA is a leading global provider of advanced ana...