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Nsure Jobs (NOW HIRING)

Kids for the Future

LA · On-site

$250 - $450/hr

E nsure manufacturing capacity, labor resources, and operational systems support business growth. * D rive improvements in throughput, efficiency, automation, andutilization. * E stablishscalable ...

Integer

Quality Technician II

Clarence, NY · On-site

$17 - $23/hr

E nsure or E stablish C ontrols for P roducts and P rocesses * Compiles or completes quality records, reports, and/or documentation ensuring GDP (Good Documentation Practices) are applied.

Worth Credit Union

Underwriter III

Bedford, TX · On-site

$60 - $90/hr

... nsure compliance with all applicable federal and state lending regulations Requirements and qualifications: * 2 to 4 years of direct loan underwriting experience in a financial institution ...

New

Smithfield Foods, Inc.

$75 - $95/hr

You will **e**nsure maintenance tasks comply with USDA regulations. Maintain accurate records of maintenance work performed and inventory.* **Crisis Management & Continuity:** In the absence of key ...

New

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Nsure information

What is the difference between Nsure vs Insurance Agent?

AspectNsureInsurance Agent
CredentialsMay require licensing, certifications depending on services offeredTypically requires state licensing and certifications
Work EnvironmentOften operates online or through brokerage platformsWorks directly with clients, in offices or remotely
Industry UsageUsed in insurance brokerage, consulting, and online platformsCommonly employed in direct sales and client consultations

While both Nsure and Insurance Agents operate within the insurance industry, Nsure often refers to online platforms or brokerage services, whereas Insurance Agents typically work directly with clients to sell insurance policies. The main differences lie in their work environment and the way they interact with clients, with Nsure leaning towards digital and brokerage services, and Insurance Agents focusing on direct sales and client relationships.

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Infographic showing various Nsure job openings in the United States as of August 2026, with employment types broken down into 96% Full Time, and 4% Part Time. Highlights an 96% Physical, and 4% Remote job distribution.

Clinical Research Safety Associate - Hybrid, Miami FL

The University of Miami

Miami, FL • On-site

Full-time

Medical, Dental

This job post has expired today. Applications are no longer accepted.

University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

265th of 629 rated colleges and universities

Job description

Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.
The Department of Executive Dean of Research is currently seeking a Clinical Research Safety Associate to work in Miami.
CORE JOB SUMMARY
The Clinical Research Safety Associate (CRSA) supports and assists with safety management and reporting of University of Miami sponsored clinical trials within the Investigator-Initiated Trial Services at the University of Miami. This role involves reviewing and evaluating serious adverse event reports (SAERs) and Adverse Events of Special Interest (AESI) to ensure compliance with regulatory reporting requirements, maintaining adverse event data in safety databases, and drafting narratives. Responsibilities include collaborating with stakeholders to gather additional safety information, preparing regulatory safety reports, monitoring safety literature, and contributing to developing safety policies and risk management plans. The CRSA works closely with clinical research, regulatory affairs, and pharmacovigilance teams to maintain the safety and compliance of investigational products.
CORE RESPONSIBILITIES
  • Review and evaluate Serious Adverse Event Reports (SAERs) and Adverse Events of Special Interest (AESIs) for compliance with regulatory reporting and funding entity requirements.
  • nsure that reported SAER and AESI event reports are received, tracked, evaluated, processed and distributed/submitted in an efficient and timely manner, and in compliance with regulations, funding entities requirements and IITS-U Safety Management Plans/SOPs.
  • Generate appropriate queries for study teams to complete and clarify SAE information as needed.
  • Ensure consistency in investigator causality assessment of SAERs, source documentation, and Reportability Assessment Forms (RAFs) for completeness, accuracy and legibility.
  • Maintain accurate and up-to-date safety information in safety databases and trackers to ensure proper documentation for audits and inspections.
  • Draft comprehensive and clear narratives for adverse events to support regulatory submission and study records.
  • Prepare safety reports, including MedWatch and CIOMS forms, for submission to regulatory authorities and funding entities in a timely and accurate manner.
  • Prepare safety documentation using requested format by funding entity.
  • Create and maintain study-specific SAE or AESI forms for study use.
  • Draft and maintain study specific comprehensive safety management plans, including workflow creation, for investigator-initiated trials to ensure consistent safety oversight.
  • Contribute to the creation and refinement of safety Standard Operating Procedures (SOPs) and risk management plans to align with Good Clinical Practices.
  • Assist with training of study team members on the safety reporting expected for the study, including how to complete SAE and/or AESI forms, timelines associated with completing the forms, and how to respond to associated queries on the data submitted.
  • Participate in the standardized set-up of new safety databases.
  • Help in compiling safety data required for Project Status Reports, DSMC meetings and other requests as applicable.
  • Perform SAE reconciliation.
  • Liaise with other units and departments.
  • Participate in inspection-readiness activities including documentation needed for eTMF.
  • Support the Medical Monitor in the review and development of written materials including clinical trial protocols, SAE and AESI reporting forms, and Reportability Assessment Forms.
  • Inform study team of safety related issues and potential trends and or signals arising from review of data

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities, as necessary.
CORE QUALIFICATIONS
Education:
Bachelor's degree in health care, science or related field required. Master's degree or higher preferred.
Certification and Licensing:
Clinical research certification (e.g. ACRP, SOCRA) preferred
Experience:
Minimum 4 years of experience with clinical trials (involving drugs, biologics or devices) required. Experience working as a clinical research monitor preferred
Knowledge, Skills and Attitudes
  • Strong knowledge of Good Clinical Practice (GCP), FDA regulatory requirements and ICH-GCP guidelines
  • Excellent English skills, both verbal and written
  • Excellent interpersonal and team skills
  • Strong attention to detail, time/project management and organization skills
  • Strong Microsoft Office (Excel, Outlook, PowerPoint, Word) skills
  • Proficiency in medical data analysis and interpretation.
  • Proficiency in using clinical trial management software.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full time
Employee Type:
Staff

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About University of Miami

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The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Coral Gables, FL, US

Year founded

1925

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