Top 31 Research 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
Quality Assurance Coordinator (Clinical Research)
Research Centers of America —Hollywood, FL
- Full-time
- Background check
- Spanish
- Psychiatry
- Health savings account
- Health insurance
Quick Apply
Clinical Research Coordinator
BRCR Global —Plantation, FL
- Full-time
- Background check
- English
- In-person
- 401(k)
- Paid time off
Quick Apply
14d
Clinical Research Coordinator
Segal Institute for Clinical Research —Lauderhill, FL
- Full-time
- Vital signs
- Psychiatry
- Addiction Medicine
- Health insurance
- Dental insurance
Quick Apply
7d
Research Coordinator II – Regulatory (DDI)
Cleveland Clinic —Weston, FL
- $47,530 - $72,475 a year
- Full-time
- Word processing
- Computer literacy
- Mid-level
- Dental insurance
- Vision insurance
Clinical Research Coordinator 1
Alliance For MultiSpecialty Research LLC —Doral, FL
- Overtime
- Vital signs
- English
- Mid-level
Quick Apply
Clinical Research Coordinator
SRA Trials —Miami, FL
- $57,000 - $70,000 a year
- 8 hour shift
- Spanish
- Vital signs
- English
- Health savings account
- Health insurance
Quick Apply
Certified Research Coordinator (CRC)
HEALING TOUCH C & C,INC —Hialeah, FL
- $25 - $30 an hour
- Full-time
- Spanish
- English
- Mid-level
Quick Apply
2d
Clinical Research Coordinator
Center for Diabetes Obesity and Metabolism INC —Pembroke Pines, FL
- Temporary
- Spanish
- Laboratory experience
- English
- Paid time off
Quick Apply
2d
Assistant Clinical Research Coordinator
Evolution Research Group —Miami, FL
- $22.00 - $26.50 an hour
- Full-time
- OSHA
- BLS Certification
- HIPAA
- Continuing education credits
- Health insurance
Quick Apply
14d
Research Nurse Coordinator - Oncology/Hematology
Cleveland Clinic —Weston, FL
- Full-time
- Hybrid work
- Nursing
- Patient monitoring
- RN License
Clinical Research Coordinator
Indago Research & Health Center, Inc —Miami Lakes, FL
- $23 - $30 an hour
- Weekends as needed
- Background check
- Spanish
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
6d
Clinical Research Coordinator (CRC) – Full-Time
Paradise Health Research —Doral, FL
- Full-time
- Spanish
- Psychiatry
- English
Quick Apply
4d
Temporary Research Program Coordinator
Florida International University —Miami, FL
- $24 an hour
- Temporary
- Mid-level
- University
- Bachelor's degree
- Mileage reimbursement
- Dental insurance
14d
Coordinator Administrative Services - Applied Research Center
Florida International University —Miami, FL
- $40,000 - $48,000 a year
- Online Application
- Background check
- Mid-level
- Office
Temporary Research Coordinator
Florida International University —Miami, FL
- $22 an hour
- Temporary
- Background check
- Spanish
- Management
- Dental insurance
- Tuition reimbursement
Program Coordinator - Center Labor Research Studies
Florida International University —Miami, FL
- $40,000 - $45,000 a year
- Online Application
- Background check
- Mid-level
- University
14d
Assistant Clinical Research Coord.
SRA Trials —Miami, FL
- $20.00 - $22.50 an hour
- 8 hour shift
- Spanish
- Nursing
- English
- Health insurance
- Dental insurance
Quick Apply
Temporary Program Coordinator
Florida International University —Miami, FL
- $19 - $25 an hour
- Temporary
- Classroom
- Management
- Mid-level
- Dental insurance
- Tuition reimbursement
2d
Bilingual Activities Coordinator
Quotient Sciences —Miami, FL
- Full-time
- 18 years or older
- Spanish
- English
Quick Apply
3d

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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

research coordinator jobs in weston fl

Regulatory Coordinator

Quality Assurance Coordinator (Clinical Research)

Clinical Research Coordinator

Clinical Research Coordinator

Research Coordinator II – Regulatory (DDI)

Clinical Research Coordinator 1

Clinical Research Coordinator

Certified Research Coordinator (CRC)

Clinical Research Coordinator

Assistant Clinical Research Coordinator

Research Nurse Coordinator - Oncology/Hematology

Clinical Research Coordinator

Clinical Research Coordinator (CRC) – Full-Time

Temporary Research Program Coordinator

Coordinator Administrative Services - Applied Research Center

Temporary Research Coordinator

Program Coordinator - Center Labor Research Studies

Assistant Clinical Research Coord.

Temporary Program Coordinator

Bilingual Activities Coordinator

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