Skip to main content
Loading
loadingbar
Loading, Please wait..!!

Regulatory Research Coordinator

  • Regulatory Research Coordinator job type Posted on: Nov 01, 2026
  • Regulatory Research Coordinator experience level Mount Sinai Medical Center
  • Regulatory Research Coordinator employment type Miami Beach, Florida
  • Regulatory Research Coordinator employment type Onsite
  • Regulatory Research Coordinator salary Full-time

Point Apply Here APPLY LATER

Curious about compensation?

Explore the historical salary trends, average pay, and estimated compensation for Regulatory Research Coordinator roles in Florida.

View Salary Guide →

Job Title :

Regulatory Research Coordinator

Job Type :

Full-Time

Job Location :

Miami Beach Florida United States

Remote :

No

Jobcon Logo Job Description :

Position ResponsibilitiesFacilitates the opening of cancer clinical research protocols.Prepares forms and informed consents for submission to MSMC Institutional Review Board.Prepares regulatory packages for the study sponsors.Organizes study initiations at MSMC and MS-Aventura.Coordinates monitoring visits by study sponsors at MSMC and MS-Aventura.Assists clinical staff in answering queries from study sponsors.Creates regulatory and protocol files for cancer studies.Keeps all regulatory binders/files organized and updated.Submits study amendments, revisions, and updates as needed to the IRB.Coordinates the distribution of newly activated protocols and protocol consent changes/updates to appropriate sites.Submits annual reviews for cancer studies to IRB.Reports adverse events to appropriate entities according to IRB and study sponsor guidelines.Assists with preparation for NCI and FDA audits.Sets up and maintain a tracking log of all submitted/approved IRB documents.Performs ad hoc duties for physician participation in NCI studies.Prepares submissions to the FDA for IND status.Assists Coordinator of Quality Assurance and Data Management in preparing protocol version and consent tracking documents.Acts as resource for research staff and physicians with regard to regulatory requirements.Coordinates activities of study sponsors with physicians and clinical research staff as needed.Performs all assigned tasks including clerical duties (answering telephones, typing, ordering supplies) to assist clinical staff, when required.Assists physicians in manuscript preparation, as required.QualificationsLicense/Registration/Certification: Not applicableEducation: Bachelors Degree preferredExperience: Regulatory experience preferredBenefitsWe believe in the physical and mental well-being of our employees and are committed to offering comprehensive benefits that fit their personal needs:Health benefitsLife insuranceLong-term disability coverageHealthcare spending accountsRetirement planPaid time offPet InsuranceTuition reimbursementEmployee assistance programWellness programOn-site housing for select positions and more!

Jobcon Logo Position Details

Posted:

Nov 01, 2026

Reference Number:

13695_U-131780172839

Employment:

Full-time

City:

Miami Beach

Job Origin:

APPCAST_CPC

Share this job:

  • linkedin

Jobcon Logo
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Regulatory Research Coordinator    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Position ResponsibilitiesFacilitates the opening of cancer clinical research protocols.Prepares forms and informed consents for submission to MSMC Institutional Review Board.Prepares regulatory packages for the study sponsors.Organizes study initiations at MSMC and MS-Aventura.Coordinates monitoring visits by study sponsors at MSMC and MS-Aventura.Assists clinical staff in answering queries from study sponsors.Creates regulatory and protocol files for cancer studies.Keeps all regulatory binders/files organized and updated.Submits study amendments, revisions, and updates as needed to the IRB.Coordinates the distribution of newly activated protocols and protocol consent changes/updates to appropriate sites.Submits annual reviews for cancer studies to IRB.Reports adverse events to appropriate entities according to IRB and study sponsor guidelines.Assists with preparation for NCI and FDA audits.Sets up and maintain a tracking log of all submitted/approved IRB documents.Performs ad hoc duties for physician participation in NCI studies.Prepares submissions to the FDA for IND status.Assists Coordinator of Quality Assurance and Data Management in preparing protocol version and consent tracking documents.Acts as resource for research staff and physicians with regard to regulatory requirements.Coordinates activities of study sponsors with physicians and clinical research staff as needed.Performs all assigned tasks including clerical duties (answering telephones, typing, ordering supplies) to assist clinical staff, when required.Assists physicians in manuscript preparation, as required.QualificationsLicense/Registration/Certification: Not applicableEducation: Bachelors Degree preferredExperience: Regulatory experience preferredBenefitsWe believe in the physical and mental well-being of our employees and are committed to offering comprehensive benefits that fit their personal needs:Health benefitsLife insuranceLong-term disability coverageHealthcare spending accountsRetirement planPaid time offPet InsuranceTuition reimbursementEmployee assistance programWellness programOn-site housing for select positions and more!

Loading
Please wait..!!