Top 75 International travel coordinator Jobs in Weston, Fl

Regulatory Coordinator
CenExel Clinical Research —Hollywood, FL
- Overtime
- Background check
- Microsoft Excel
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Site Director
Evolution Research Group —Miami, FL
- $175,000 - $200,000 a year
- Full-time
- Bachelor of Science
- HIPAA
- 3 years
- Health insurance
- Dental insurance
Quick Apply
Group Services Coordinator
HA Group —Fort Lauderdale, FL
- Full-time
- Hybrid work
- Sales
- Mid-level
- Office
- Employee stock purchase plan
- Health insurance
Quick Apply
14d
Site Coordinator/Psychometrist
NEUROCOGNITIVE SPECIALTY GROUP —Fort Lauderdale, FL
- $23.00 - $26.50 an hour
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Paid holidays
- Health insurance
Quick Apply
Operations Coordinator
GCL —Doral, FL
- Overtime
- Microsoft Outlook
- Customer service
- Research
- Continuing education credits
- Paid parental leave
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13d
Crew Coordinator
Fraser Yachts —Fort Lauderdale, FL
- Microsoft Outlook
- Computer literacy
- Mid-level
Hospitality Coordinator - PS MIA
Extime PS LLC —Miami, FL
- Weekends as needed
- Background check
- Pass drug screening
- Research
- Paid training
- Health savings account
Quick Apply
5d
Technology Coordinator - Information Technology
001 Seminole Hard Rock Hollywood —Hollywood, FL
- Full-time
- Microsoft Excel
- Basic math
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Vision Mission Trip Leader, Travel Analyst
Cross Catholic Outreach —Pompano Beach, FL
- $76,000 - $90,000 a year
- Full-time
- Hybrid work
- Bilingual
- Background check
- Spanish
- Wellness program
- Health savings account
Quick Apply
10d
Bilingual German/English Customer Service Representative
Redion —Pembroke Pines, FL
- Overtime
- Hybrid work
- 1 year
- Communication skills
- Entry level
- Travel reimbursement
- Paid parental leave
Quick Apply
9d
Case Management Coordinatore
REVA Air Ambulance —Fort Lauderdale, FL
- $60,000 - $90,000 a year
- Full-time
- Microsoft Outlook
- Customer service
- Computer literacy
Quick Apply
Senior Fleet Employee Experience Specialist
Princess Cruise Line —Fort Lauderdale, FL
- Full-time
- Hybrid work
- Microsoft Word
- Writing skills
- Mid-level
- Employee stock purchase plan
- Health insurance
Quick Apply
6d
Crew Coordinator Supervisor
Fraser Yachts —Fort Lauderdale, FL
- Hybrid work
- Microsoft Outlook
- Computer literacy
- Mid-level
Quick Apply
Project Manager, Cruise
DSV —Medley, FL
- $71,000 - $89,000 a year
- Email
- Microsoft Excel
- Construction site
- 5 years
Temporary Program Coordinator
Florida International University —Miami, FL
- $19 - $25 an hour
- Temporary
- Classroom
- Management
- Mid-level
- Dental insurance
- Tuition reimbursement
Research Coordinator I - Center for Children and Families
Florida International University —Miami, FL
- $40,000 - $45,000 a year
- Weekends as needed
- Background check
- Mid-level
- University
10d
Senior Coordinator Administrative Services
Florida International University —Miami, FL
- $55,000 - $62,000 a year
- Online Application
- Background check
- Office
- 3 years
4d
Brand Image Manager, Wholesale, South Florida
Ralph Lauren —Aventura, FL
- Weekends as needed
- Microsoft Outlook
- Computer literacy
- Research
Executive Operations Coordinator
FasterPay —Miami Beach, FL
- $50,786.79 - $62,366.88 a year
- Full-time
- ERP systems
- Mid-level
- Office
Quick Apply
12d
Health Technician (Orthotic Fitter)
US Veterans Health Administration —Broward County, FL
- $53,740 - $69,864 a year
- Online Application
- Background check
- Psychiatry
- Pass drug screening

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Regulatory Coordinator

CenExel Clinical Research -
Hollywood, FL

Quick Apply

Job Details

Full-time

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Vision insurance
401(k) matching
Life insurance

Qualifications

Computer operation
Microsoft Excel
Clinical research
Word processing
Writing skills
Drug regulation
High school diploma or GED
Regulatory affairs
Typing

Full Job Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

With moderate oversight the Regulatory Coordinator I is responsible for the preparation, organization and implementation of regulatory research documents such as pre-study activities, initiation, execution, and reporting on the various status of research tasks in accordance with FDA guidelines, ICH GCP and SOPs. Maintain regulatory documents in accordance with applicable regulations and coordinate required investigator and study staff training.

Essential Responsibilities and Duties:

Collects, prepares, and submits documentation to various sponsors/CROs during study start-up, including:
o Submission documents/approvals
o Protocol amendments with respective signature pages
o Informed consent documents
o FDA form 1572
o Lab normal result documents
o financial disclosure forms
o Delegation of authority logs
o Licenses
o Reports
o Logs (e.g., temperature logs, drug accountability logs, master subject logs, screening and enrollment logs, specimen logs, etc.)
Collects, prepares, and submits documentation to institutional review boards for all ongoing and new trials.
Serve as a liaison between the IRB, site, and investigator.
Obtain necessary signatures from investigators and staff.
Maintains and tracks current staff credentials (i.e., CV, certifications, etc.)
Maintains and distributes new and revised regulatory documents to applicable site staff and applicable corporate teams.
Refers necessary regulatory questions to Sr. Regulatory Coordinator, Regulatory Manager or Regional Regulatory Manager.
Maintains regulatory documents for ongoing trials, and ensures all appropriate regulatory documents are archived at the conclusion of the study.
Submits applicable subject facing documents for translations.
Maintains current Clinical Conductor Regulatory information.
Prepares appropriate reports for submission as required to the IRB including Serious Adverse Events (SAE’s), protocol deviations and other required reports.
Completes onboarding of new Investigators, including CV creation, obtaining medical license, and training documents.
Ensures the regulatory binder is ready for monitor review during monitor visits. Meets with monitor, as necessary.
Assists with regulatory inspections and sponsor audits as necessary.
Performs close-out duties including preparing the final report to the IRB and ensuring all original documents are filed in the regulatory binder. Ensures all appropriate regulatory documents are archived at the conclusion of the study.
Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

Must be a high school graduate or have GED equivalency.
0-2 years of experience in clinical research regulatory affairs.
Demonstrated prioritization and organizational skills to efficiently and effectively, providing accurate information in a timely manner.
Ability to prioritize workload to meet demands of PI, coordinators, sponsors, and IRBs.
Demonstrated interpersonal skills to work with physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
Ability to understand work may be delegated by more than one person, depending on the individual needs of the clinical study and to carry out job responsibilities as assigned in a timely manner.
Computer skills using PC platform computers with proficiency in Excel and Word to enter data and generate correspondence accurately.
Ability to learn and become proficient in eRegulatory systems, IRB portals, vendor portals and sponsor portals.
A critical thinker with strong attention to detail and superb problem-solving abilities.
Must be able to effectively communicate verbally and in writing.

Working Conditions

Indoor, Office environment.
Essential physical requirements include sitting, typing, standing, and walking.
Lightly active position, occasional lifting of up to 20 pounds.
Reporting to work, as scheduled, is essential.
Ability to work overtime, weekends, and/or holidays as needed.
Ability to travel as needed.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Benefits:

401(k) matching
Dental insurance
Flexible spending account
Health insurance
Health savings account
Life insurance
Vision insurance

Experience:

Clinical research: 1 year (Required)
Regulatory : 1 year (Required)

Work Location: In person

Quick Apply

Refine Your Search

international travel coordinator jobs in weston, fl

Regulatory Coordinator

Site Director

Group Services Coordinator

Site Coordinator/Psychometrist

Operations Coordinator

Crew Coordinator

Hospitality Coordinator - PS MIA

Technology Coordinator - Information Technology

Vision Mission Trip Leader, Travel Analyst

Bilingual German/English Customer Service Representative

Case Management Coordinatore

Senior Fleet Employee Experience Specialist

Crew Coordinator Supervisor

Project Manager, Cruise

Temporary Program Coordinator

Research Coordinator I - Center for Children and Families

Senior Coordinator Administrative Services

Brand Image Manager, Wholesale, South Florida

Executive Operations Coordinator

Health Technician (Orthotic Fitter)

I want to receive the latest job alert for international travel coordinator in weston, fl

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