Clinical Research Coordinator I - Sarasota

The Clinical Research Coordinator prepares regulatory submissions to IRB and sponsors, · coordinates multiple study projects, audits data submission, · and advises patients on trial design.This role requires research certification within one year of eligibility · and a minimum of ...

+Prepares and submits regulatory submission to IRB and sponsors, documentation compliance for multiple study projects, audit preparation, and data submission. · +Require research certification within one (1) year of eligibility. · Require a minimum of five (5) years of healthcare ...

Prepares and submits regulatory submission to IRB and sponsors, documentation compliance for multiple study projects, audit preparation, and data submission. This position also will be responsible for advising patients of trial design, facilitating informed consent for investigat ...

Prepares and submits regulatory submission to IRB and sponsors documentation compliance for multiple study projects audit preparation and data submission This position also will be responsible for advising patients of trial design facilitating informed consent for investigators f ...

We believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, · tuition reimbursement, ...

The Clinical Research Coordinator I is responsible for coordinating all aspects of assigned research projects facilitated by the assigned PI. · ...

We believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training and competitive wages. · ...

The Clinical Research Coordinator III RN position at Florida Cancer Specialists & Research Institute involves implementing research studies under medical supervision and managing site operations. · Responsible for performance of research study under medical supervision. · May pro ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. · ...

+Join the team that is revolutionizing health care -- BayCare Health System. This position involves leading and implementing clinical trials under the direction of a Principle Investigator. · ...

At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. · Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director. · ...

At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them.In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, tra ...

A Clinical Research Coordinator/Register Nurse will assist in protocol review and study start-up activities, prepare regulatory documents for IRB/EC submission, recruit participants according to inclusion/exclusion criteria, · obtain informed consent, collect and record study dat ...

+ Clinical Research Coordinator/RN- ASI · The Clinical Research Coordinator (CRC) is responsible for managing and coordinating the day-to-day activities of clinical trials. This role ensures compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP ...

The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol,FDA Regulations,and ICH/GCP guidelines and to provide the best quality data to the sponsor. · Comple ...

The Clinical Research Regulatory Coordinator I for Study Activation will be responsible for ensuring that accurate and upto-date regulatory files are maintained for all pediatric clinical research studies.This person will serve as a central resource for faculty conducting interve ...

The Clinical Research Regulatory Coordinator I will be responsible for ensuring that accurate and upto-date regulatory files are maintained for all pediatric clinical research studies. This person will serve as a central resource for faculty conducting interventional and non-inte ...

This position is fully on-site, no option for remote. · ...

Responsible for writing and applying for research specific grants to support unfunded or under-funded initiatives of the Research Division. · ...

The Director of Scholarly Programs and Education is responsible for shaping and helping to lead overall research identity multi-year research agenda Elling Eide Center Sarasota Florida. · We seeking rare individual help advance approach scholarship provides students scholars uniq ...