Top 17 Qa auditor i Jobs in Miami Fl

Clinical Research Coordinator
Segal Institute for Clinical Research —North Miami, FL
- Full-time
- Bilingual
- Vital signs
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
QA Auditor I
AVEVA DRUG DELIVERY SYSTEMS INC —Miramar, FL
- $25 an hour
- Microsoft Excel
- English
- Mid-level
Research Quality Assurance Auditor
University of Miami —Coral Gables, FL
- Full-time
- Hybrid work
- English
- Mid-level
- Master's degree
Quality Assurance Auditor
Global Crossing Airlines —Miami, FL
- Full-time
- Ability to walk for extended periods
- Mid-level
- Office
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QA ADMINISTRATIVE ASSISTANT
Commercial Jet, Inc —Miami, FL
- Spanish
- English
- Mid-level
Quick Apply
Auditor
Univista Insurance —Miami, FL
- $17 - $20 an hour
- Microsoft Excel
- Mid-level
- Analysis skills
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Quality Auditor
H&H —Fort Lauderdale, FL
- Full-time
- Computer science
- Computer Science
- Office
- 401(k)
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Quality Manager
MD Turbines Inc —Hialeah, FL
- Full-time
- 5 years
- Analysis skills
- Warehouse
Quick Apply
Fleet Installation Quality Inspector
The PAC Group —Pembroke Pines, FL
- $38.50 - $45.45 an hour
- Temporary
- Mid-level
- Ability to climb stairs
- Leadership
Quick Apply
Safety Inspector (2nd shift)
AAR Corp. —Miami, FL
- Full-time
- Mechanic experience
- Customer service
- 5 years
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Governance Senior Specialist
Olympus —Miami, FL
- Hybrid work
- Spanish
- Computer literacy
- English
- Paid parental leave
- Paid holidays
Benefits Analyst
Southern Glazer’s Wine and Spirits —Miramar, FL
- Extended hours
- Research
- Mid-level
- Office
- Wellness program
- Disability insurance

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Clinical Research Coordinator

Segal Institute for Clinical Research -
North Miami, FL

Quick Apply

Job Details

Full-time

Benefits

Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Employee discount
Life insurance
Referral program

Qualifications

Bilingual
CCRC
Clinical research
Clinical trials
CCRP
Documentation review

Full Job Description

The Clinical Research Coordinator is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the vision and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned trials. The CRC follows study specific protocol guideline and communicates and interacts with Investigators, clinic staff, CROs and Sponsors to effectively perform clinical research and coordinate research activities. All duties carried out by the CRC are done in accordance with company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable local, state, and federal regulations.

Primary Responsibilities

· Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.

· Identify potential problems or inconsistencies and take action as appropriate.

· Articulate protocol issues to CRO and/or Sponsor, Site Lead, Manager, Principal or Sub-Investigator, and other members of the study team.

· Collect initial subject health and demographic information by interviewing subjects and accessing other appropriate sources.

· Review subject comprehensive medical documentation to determine protocol eligibility under the supervision of the Principal Investigator.

· Ensure a flow of communication including telephone conferences between subject, study staff, referral sources and recruitment team, Sponsor and/or CRO, Monitor(s) and Auditors, if applicable.

· Perform clinical tasks including, but not limited to vital signs, height and weight, ECG, phlebotomy, specimen processing and packaging.

· Dispense and maintain accurate records of investigational and study product.

· Educate subject and family members regarding specific studies and clinical drug trials in general.

· Complete all monitor and sponsor queries in a timely manner.

· Perform some phlebotomy

· Perform Quality Control (QC) checks on all trials per company SOP and interface with QA Director as needed

Recruitment Responsibilities

· Provide weekly updates to Active Studies Report
· Communicate all advertising needs to recruitment team
· Maintain weekly communication with recruitment team to maximize recruitment in all enrolling trials

Minimum Qualifications:

At least 2 yrs of experience as a CRC in clinical research or relevant clinical role
CCRC or CCRP certification preferred

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Report to duty at physical locations other than the primary assigned location(s) on an as-needed basis. The fluctuating nature of the industry and the existence of multiple physical business addresses mean that employees must be prepared to adjust work location within reason as dictated by business needs.

Job Type: Full-time

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Employee discount
Flexible spending account
Health insurance
Life insurance
Paid time off
Referral program
Vision insurance

Ability to Commute:

North Miami, FL 33161 (Required)

Ability to Relocate:

North Miami, FL 33161: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Refine Your Search

qa auditor i jobs in miami fl

Clinical Research Coordinator

QA Auditor I

Research Quality Assurance Auditor

Quality Assurance Auditor

QA ADMINISTRATIVE ASSISTANT

Auditor

Quality Auditor

Quality Manager

Fleet Installation Quality Inspector

Safety Inspector (2nd shift)

Governance Senior Specialist

Benefits Analyst

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