Regulatory Research Coordinator

Posted 4 Days Ago
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Miami Beach, FL, USA
In-Office
Entry level
Healthtech
The Role
Coordinates regulatory activities for cancer clinical research protocols, including IRB and FDA submissions, informed consents, sponsor packages, monitoring visits, regulatory files, amendments, annual reviews, adverse-event reporting, audit preparation, and protocol tracking. Supports physicians, clinical staff, study sponsors, and research teams while performing related administrative and manuscript-preparation duties.
Summary Generated by Built In

As Mount Sinai grows, so does our legacy in high-quality health care.

Since 1949, Mount Sinai Medical Center has remained committed to providing access to its diverse community. In delivering an unmatched level of clinical expertise, our medical center is committed to recruiting and training top healthcare workers from across the country. We offer the latest in advanced medicine, technology, and comfort in 12 facilities across Miami-Dade (including our 674-bed main campus facility) and Monroe Counties, with 38 medical services, including cancer care, 24/7 emergency care, orthopedics, cardiovascular care, and more. Mount Sinai takes pride in being South Florida's largest private independent not-for-profit hospital, dedicated to continuing the training of the next generation of medical pioneers.

Culture of Caring: The Sinai Way

Our hardworking, tight-knit community of more than 4,000 dedicated employees fosters an environment of care and compassion. Each member plays a vital role in our collective mission to deliver excellent healthcare through innovation, education, and research. At Mount Sinai, we take pride in our achievements, aiming to be a beacon of quality healthcare in South Florida. We welcome all healthcare professionals to join our thriving community and contribute to our pursuit for clinical excellence.

Department:

Job Description Summary:

Position Responsibilities
  • Facilitates 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.
Qualifications
  • License/Registration/Certification
    • Not applicable
  • Education
    • Bachelors Degree preferred
  • Experience
    • Regulatory experience preferred

Benefits:

We believe in the physical and mental well-being of our employees and are committed to offering comprehensive benefits that fit their personal needs:

  • Health benefits
  • Life insurance
  • Long-term disability coverage
  • Healthcare spending accounts
  • Retirement plan
  • Paid time off
  • Pet Insurance
  • Tuition reimbursement
  • Employee assistance program
  • Wellness program
  • On-site housing for select positions and more!

Degree Requirements:

Certification:

Skills Required

  • Bachelor's degree
  • Regulatory experience
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The Company
HQ: Miami Beach, FL
4,000 Employees
Year Founded: 1949

What We Do

Mount Sinai Medical Center is a private, independent, not-for-profit teaching hospital serving South Florida. Established in 1949, it provides advanced medical care through 12 facilities and 38 services, including cancer, emergency, orthopedic, and cardiovascular care. Its mission emphasizes excellent healthcare for a diverse community through clinical expertise, innovation, education, research, charity care, and financial responsibility, while training the next generation of healthcare professionals.

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