Top 34699 Research Worker Jobs

Regulatory Specialist
Indago Research & Health Center —Miami Lakes, FL
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- Weekends as needed
- Background check
- Spanish
- English
- Paid holidays
- Disability insurance
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Research Senior Scientific Director, Head of Hit ID and Sample Management (Automation)
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Research Worker
Columbia University —New York, NY
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Research Associate I- Alexanian Lab
Gladstone Institutes —San Francisco, CA
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Student Research Worker
Columbia University —New York, NY
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Research Specialist I
University of Rochester —Rochester, NY
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Tetra Tech —Denver, CO
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RESEARCH
The University Of Denver —Denver, CO
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Retail Professionals
Handshake AI —Remote
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Bacteriophage Research Scientist - Kennesaw, GA
ADM —Kennesaw, GA
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- Overtime
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14d
Temporary Research Assistant, Economic Dignity Lab
Georgetown University —Washington, DC
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- Analysis skills
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- Bachelor's degree
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Research Assistant
RHSC —Saint Paul, MN
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- Weekends as needed
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10d
Community Health Worker Certified-1
Geisinger —Remote
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Research Specialist - Emory Primate Center
Emory University —Atlanta, GA
- Full-time
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Research Assistant 2
Oregon Health & Science University —Portland, OR
- $48,214.40 - $68,681.60 a year
- Full-time
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Community Health Worker Certified-2
Geisinger —Remote
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Research Associate
University of Texas at Austin —Austin, TX
- From $90,000 a year
- Urgently hiring
- Office
- University
- Doctor of Philosophy
- Retirement plan

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Regulatory Specialist

Indago Research & Health Center -
Miami Lakes, FL

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Job Details

Full-time
$24 - $31 an hour

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Military leave
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Bereavement leave
Life insurance
Referral program

Qualifications

Spanish
Filing
English
Attention to detail
Organizational skills
Associate's degree

Full Job Description

Job highlights:

The Regulatory Affairs Coordinator is responsible for maintaining the Regulatory Binders up to date and working closely with Sponsors, CROs, and IRBs to facilitate the timely turnaround of study documents, ensuring there is adequate Regulatory oversight. All duties are carried out in accordance with the company policies, SOPs, and Good Clinical Practice (GCP) as well as all applicable Local, State, and Federal regulations. Job functions:

Accesses the IRBs portals for daily updates.
Interacts with Sponsors/CROs and Site staff to exchange relevant information and study updates.
Work with study staff to expedite start-up activities and enhance the Site activation.
process, while ensuring all activation accesses and requirements have been met.
Collects, reviews, and submits essential Regulatory documents.
Updates Trust with updated Informed Consent Forms and Protocol Amendments.
Oversee initial submission, collection, and maintenance of central and current IRBs and documents.
Ensures filing of IRB-approved documents i.e., Protocol and Protocol amendments, Investigators Brochure, Recruitment materials, interim and approval reports, etc.
Registers and coordinates Investigators' meeting schedules, including monitors visits.
Review the Regulatory Binder before monitoring visits.
Ensures all Regulatory items are filed under the appropriate section.
Reviews Delegation of Authority logs are appropriately updated by PI’s as necessary.
Able to identify, escalate, and resolve issues before they become critical.
Proposes alternatives to improving Regulatory workflow.
Reviews 1572 FDA Form for errors.
Collects signed Financial Disclosure Forms from Investigators.
Ensures that offsite facilities working in the study are also included in the 1572and verify they receive training and accesses required by the Sponsor.
Updates Regulatory documents as needed.
Learns and utilizes various reporting tools.
Resolves all queries related to the Regulatory matters left by Clinical Research Associates within a week of them being issued.
Accurately maintains data in the Site’s system.
Provides training and assists as liaison between the Sponsors and the Clinical Research Coordinators.
Accesses Sponsor’s specific portals such as Exostar, CPAC, SIP, Clinergize, Firecrest, Investigator Space, Longboat, for new communications and INDs.
Assists with preparation for FDA Inspections, Sponsor audits, and Internal audits.
Reviews and resolves Sponsor, CRA, CRC or supervisors request in a timely manner.
Completes additional tasks as required by a specific protocol.
This position reports to the Regulatory Affairs Manager.

Desired qualifications:

Works well in a team environment.
Familiarity with Clinical Terminology preferred.
Excellent written and verbal communication skills.
High attention to detail and organization.
Clinical Research experience preferred.
Adjusts quickly to environmental changes and shifting priorities of the dynamic organization.
Bi-lingual English/Spanish required.
Ability to work after hours and weekends if needed.
Knowledge of Microsoft Office 365.

Minimum requirements:

Associate degree required; bachelor’s degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years) or equivalent combination of education, training, and experience.

Benefits:

Medical, GAP, Dental, and Vision Insurance
Life Insurance (includes Will Preparation, Employee Assistance Program (EAP), and Travel Assistance)
Short & Long-Term Disability
Workers’ Compensation Insurance
COBRA Continuation Coverage
401(k) Retirement Savings Plan with employer match up to 4%.
Paid Time Off
Paid Holidays
Bereavement Leave
Family and Medical Leave Act (FMLA)
Military Leave
Referral Program
Tuition Assistance/Professional Development
Certification Reimbursement

Job Type: Full-time

Pay: $24.00 - $31.00 per hour

Expected hours: 40.0 per week

Benefits:

401(k)
401(k) matching
Health insurance

Work Location: In person

Apply Now

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