Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Finance
Regulatory Affairs Specialist
Plantation, FL

Find & Apply For Regulatory Affairs Specialist Jobs in Plantation, Florida

Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.

Skip to job details
Now viewing: Regulatory Affairs Specialist
Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

BRCR Global

Regulatory Affairs Specialist

Job Description

Regulatory Affairs Specialist BRCR Global - 4.0 Plantation, FL Job Details Full-time $26 an hour 8 hours ago Benefits 401(k) Paid time off Qualifications Spanish Interpersonal skills Biostatistics Writing skills English Bachelor's degree Attention to detail Computer skills Full Job Description The Regulatory Affairs Specialist plays a crucial role in the clinical trial process by giving support and overseeing the daily regulatory activities by ensuring compliance with relevant regulations.
Principal Responsabilities:
Prepare and maintain complete and accurate regulatory documents in support of clinical research studies. Manage all the communication with the IRB and Sponsor. Prepare each study-specific protocol, informed consent form, HIPAA authorization and other related documents for review by the IRB. Prepare and submit amendments, yearly requests for continuing approval of open protocols, audits, deviations, adverse event reports, and any other IRB-required submissions. Work with staff members to complete Financial Disclosure Forms for each study. Assist coordinators and site leadership in tracking the training status for existing staff, assisting with updates as needed. Maintain study binder, paper or electronic as appropriate, with all IRB related documents and correspondence for each study to always ensure audit readiness. Assist site leadership and coordinators in the preparation for monitoring visits, sponsor audits, and regulatory audits by conducting quality checks of the regulatory binder. Assist with the preparation and submission of closeout documents to the sponsors and IRBs including ensuring completeness, audit-readiness, and closure of the regulatory binder and appropriate archival of trial data. Submit or support SAE and AE submissions to the IRB as needed and in a timely fashion Job requirements:
Education:
Bachelor's degree in Science or related fields.
Experience:
1 year of experience in Regulatory Affairs for Clinical Research.
Languages:
Bilingual (English and Spanish).
Skills:
Attention to details. Strong verbal and written communication skills. Problem solving. Analytical skills. Microsoft skills.
Pay:
$26.00 per hour
Benefits:
401(k) Paid time off
Experience:
Regulatory Affairs :
1 year (Preferred)
Language:
English (Preferred) Spanish (Preferred)
Work Location:
In person