Regulatory Analyst 2 - Remote

University of Miami; Miami (FL); Remote; USD 50,000 - 80,000; Full time

Job summary

An established industry player in the academic medical field is looking for a dedicated professional to join their team. This role offers a unique opportunity to engage in groundbreaking research and ensure compliance with regulatory standards. You'll be overseeing study submissions and collaborating with diverse teams, all while contributing to patient care initiatives. With a competitive salary and comprehensive benefits, this position is perfect for someone eager to grow in a supportive environment. If you're passionate about research compliance and want to make a difference, this could be your ideal role.

Benefits

Comprehensive benefits package

Tuition remission

Career advancement opportunities

Qualifications

• Bachelor's degree required with 2+ years in compliance or clinical settings.
• Strong communication and analytical skills are essential.

Responsibilities

• Oversee study submissions and maintain regulatory documents.
• Serve as contact for boards and assist with clinical trial applications.

Skills

Compliance Knowledge

Strong Communication Skills

Analytical Skills

Proficiency in Microsoft Office

Proficiency in Adobe Acrobat

Education

Bachelor's Degree in a relevant field

Tools

Microsoft Office

Adobe Acrobat

Job description

Employer Industry: Academic Medical Center

Why consider this job opportunity:
- Competitive salary and comprehensive benefits package including medical, dental, and tuition remission
- Opportunity for career advancement and growth within the organization
- Engage with diverse boards, committees, and sponsors in the clinical research field
- Work in a collaborative environment focused on compliance and regulatory oversight
- Chance to contribute to groundbreaking research and patient care initiatives

What to Expect (Job Responsibilities):
- Oversee and support the process of study submissions and regulatory document maintenance
- Serve as the point of contact for various boards, committees, and sponsors
- Assist in the submission of applications for institutional clinical trials
- Draft, prepare, and present programs to raise awareness of research compliance
- Maintain current knowledge of applicable regulatory topics and ensure compliance with regulations

What is Required (Qualifications):
- Bachelor's Degree in a relevant field
- Minimum of two (2) years of relevant experience in compliance, research, or medical/clinical settings
- Strong written and oral communication skills
- Proficiency in Microsoft Office and Adobe Acrobat
- Knowledge of processes associated with clinical trials and applicable regulations

How to Stand Out (Preferred Qualifications):
- Certification such as SOCRA - CCRP is recommended
- Experience with IND/IDE/FDA regulations is preferred
- Strong analytical skills and ability to prioritize work under pressure

#AcademicMedicalCenter #ClinicalResearch #RegulatoryCompliance #CareerOpportunity #HealthSystem

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