Regulatory Analyst 2 - Remote

Talentify.io; United States; Remote; USD 50,000 - 90,000; Full time

Job summary

Join a forward-thinking academic medical center where you can make a real impact in clinical research and compliance. This role offers a competitive salary and comprehensive benefits, including medical and dental coverage. You will oversee study submissions, engage with diverse stakeholders, and contribute to groundbreaking research initiatives. With opportunities for career advancement and a collaborative environment, this position is perfect for those looking to grow in the clinical research field. If you are passionate about compliance and regulatory oversight, this is the opportunity for you.

Benefits

Comprehensive Benefits Package

Tuition Remission

Career Advancement Opportunities

Collaborative Work Environment

Qualifications

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

Responsibilities

• Oversee study submissions and maintain regulatory documents.
• Serve as point of contact for boards and sponsors.

Skills

Compliance Knowledge

Research Experience

Communication Skills

Microsoft Office Proficiency

Adobe Acrobat Proficiency

Analytical Skills

Education

Bachelor's Degree in 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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