Tampa, FL · On-site
$52K - $85K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Tampa, FL · On-site
$52K - $85K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Lauderdale Lakes, FL · On-site
$57.50 - $69/hr
Other duties include supervising and directing support personnel, adverse event monitoring, participating in medication use performance improvement activities, and serving as a resource for pharmacy ...
Lauderdale Lakes, FL · On-site
$57.50 - $69/hr
Other duties include supervising and directing support personnel, adverse event monitoring, participating in medication use performance improvement activities, and serving as a resource for pharmacy ...
Lauderdale Lakes, FL · On-site
$58 - $69.75/hr
Other duties include supervising and directing support personnel, adverse event monitoring, participating in medication use performance improvement activities, and serving as a resource for pharmacy ...
Lauderdale Lakes, FL · On-site
$58 - $69.75/hr
Other duties include supervising and directing support personnel, adverse event monitoring, participating in medication use performance improvement activities, and serving as a resource for pharmacy ...
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Lauderdale Lakes, FL · On-site
$57.50 - $69/hr
Other duties include supervising and directing support personnel, adverse event monitoring, participating in medication use performance improvement activities, and serving as a resource for pharmacy ...
Quick apply
Lauderdale Lakes, FL · On-site
$57.50 - $69/hr
Other duties include supervising and directing support personnel, adverse event monitoring, participating in medication use performance improvement activities, and serving as a resource for pharmacy ...
Tampa, FL · On-site
$52K - $85K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Tampa, FL · On-site
$52K - $85K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Tampa, FL · On-site
$60K - $98K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Tampa, FL · On-site
$60K - $98K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Tampa, FL · On-site
$60K - $98K/yr
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring ...
Lantana, FL · On-site
Complete incident report for any unusual or adverse event including medication errors and medication reactions. * Other duties as required to address operational needs. * Assist with additional tasks ...
New
Quick apply
Lantana, FL · On-site
Complete incident report for any unusual or adverse event including medication errors and medication reactions. * Other duties as required to address operational needs. * Assist with additional tasks ...
New
Sunrise, FL · On-site
Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint ...
Sunrise, FL · On-site
Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint ...
Lutz, FL · On-site
$85 - $110/hr
Supports physicians and facility leadership in the disclosure to patients and/or family of patients who are subject to an adverse event. * Investigates every allegation of sexual misconduct against ...
Lutz, FL · On-site
$85 - $110/hr
Supports physicians and facility leadership in the disclosure to patients and/or family of patients who are subject to an adverse event. * Investigates every allegation of sexual misconduct against ...
Supports physicians and facility leadership in the disclosure to patients and/or family of patients who are subject to an adverse event. * Investigates every allegation of sexual misconduct against ...
Supports physicians and facility leadership in the disclosure to patients and/or family of patients who are subject to an adverse event. * Investigates every allegation of sexual misconduct against ...
Report all serious adverse events immediately to the sponsor and IRB. * Ensure that the informed consent form contains all the elements required by regulatory agencies. * Obtain a signed and dated ...
Quick apply
Report all serious adverse events immediately to the sponsor and IRB. * Ensure that the informed consent form contains all the elements required by regulatory agencies. * Obtain a signed and dated ...
Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint ...
Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint ...
Plant City, FL · On-site
$65 - $80/hr
Manage and document adverse events (AEs) and serious adverse events (SAEs), escalating them to PI and sponsor as required. * Maintain GCP-compliant source notes. * Participate in investigator ...
Plant City, FL · On-site
$65 - $80/hr
Manage and document adverse events (AEs) and serious adverse events (SAEs), escalating them to PI and sponsor as required. * Maintain GCP-compliant source notes. * Participate in investigator ...
Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint ...
Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint ...
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
Tampa, FL · On-site
$60K - $98K/yr
To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
| Aspect | Adverse Event | Clinical Research Coordinator |
|---|---|---|
| Required credentials | Medical knowledge, pharmacovigilance training | Research ethics, study protocols |
| Work environment | Healthcare settings, hospitals, clinics | Research sites, hospitals, clinics |
| Employer and industry usage | Pharmaceutical companies, healthcare providers | Research institutions, hospitals |
| Common search intent | Understanding safety reporting | Managing clinical trials |
Adverse Event involves monitoring and reporting negative effects related to medical treatments, requiring medical and pharmacovigilance expertise. Clinical Research Coordinators manage and oversee clinical trials, focusing on study procedures and participant coordination. While both roles operate within healthcare and research environments, their responsibilities and required skills differ significantly.
For Adverse Event jobs in Florida, the most frequently searched job titles are:
The top searched job categories for Adverse Event jobs in Florida are:
$52K - $85K/yr
Full-time
Re-posted 19 days ago
7.3
Based on 191 frontline employees who took The Breakroom Quiz
305th of 898 rated healthcare providers
The University of Alabama at Birmingham (UAB), Neurology Chair Office, is seeking a Clinical Research Nurse Coordinator I.
The Clinical Research Nurse Coordinator II (Movement Disorders) coordinates clinical research studies focused on Parkinson's disease, Huntington's disease, and other movement disorders. This role integrates nursing expertise with research coordination responsibilities to ensure the safe and effective conduct of clinical trials and observational studies. In addition to research responsibilities, this position serves as the clinic nurse for the monthly multidisciplinary Huntington's Disease Clinic, collaborating with neurology providers and allied health professionals to coordinate patient care, provide education and support to patients and caregivers, and facilitate clinic operations.
The Clinical Research Nurse Coordinator II is responsible for participant recruitment, screening, enrollment, study visit implementation, investigational product management, adverse event monitoring, data collection, and maintenance of accurate research documentation. This position supports the advancement of innovative therapies and contributes to improved outcomes for patients with movement disorders through high-quality clinical research.
General Responsibilities
To serve as coordinator for clinical research studies and provides support to other study team members for research trials, studies, and projects within the confines of the study protocols as directed.
To support protocol screening and study participant eligibility determination, working with more senior study team members to ensure compliance.
To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP). May provide quality care to participants and their families within the area of clinical specialty.
To assist with the life cycle of the study from start-up through maintenance to closure.
To coordinate and organize participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
To perform the informed consent process following GCP.
To act as a liaison among the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.
Performs other duties as assigned.
Annual Salary Range: $52,555 - $85,400
Bachelor's degree in a related field required. Work experience may substitute for education requirement. Currently licensed or eligible to be licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.
Preferences
Organized, detail-oriented, and compassionate RN who is proficient in phlebotomy and documentation. This employee will coordinate multiple clinical trials independently.
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.
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Health care and social assistance
501 - 1,000 Employees
Birmingham, AL, US
1945
