Regulatory Specialist

Technical Resources International, Inc.; Bethesda (MD); Hybrid; USD 75,000 - 85,000; Full time

Job summary

A regulatory affairs organization in Bethesda is seeking a Regulatory Specialist to manage regulatory submissions and scientific document preparations. The role requires a Bachelor's Degree and strong communication skills. Candidates should have knowledge of Microsoft Office and GCP. This hybrid position offers 2 days on-site and 3 days remote work. The salary ranges from $75,000 to $85,000 annually.

Qualifications

• Excellent oral and written communication skills; detail-oriented.
• Ability to analyze medical research data and review protocols.
• Experience in preparing regulatory documents and submissions.

Responsibilities

• Prepare and track regulatory submissions including INDs and BLAs.
• Prepare scientific documents for the FDA and other Health Authorities.
• Attend scientific meetings to stay updated on developments.

Skills

Excellent oral and written communication skills

Detail-oriented and able to multi-task/prioritize

Ability to analyze medical research data

Strong working knowledge of Microsoft Office

Familiarity with GCP

Education

Bachelor's Degree

Tools

Microsoft Office

SharePoint

Job description

Regulatory Specialist - (RS001_COMPANY_1.5)

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Job Title

Regulatory Specialist

Location

Bethesda, MD 20817 US (Primary)

Category

Regulatory Affairs

Job Type

Full-Time

Salary Range

75,000.00-85,000.00/YEAR

Education

Bachelor\'s Degree

Travel

None

Job Description

• Prepare, distribute, and track regulatory submissions including, drug and biologic Investigational New Drug Applications (INDs), Biologics License Application (BLAs), New Drug Application (NDAs), Investigational Device Exemption (IDEs), ensuring compliance in accordance with GCPs/ICH and all applicable FDA/other Regulatory Health Authority regulations.
• Prepare scientific and other regulatory documents for submission to the Food and Drug Administration (FDA) and other Health Authorities.
• Attend scientific meetings and reviews the literature to stay current with new developments in the infectious disease field (in particular, human immunodeficiency virus (HIV) and tuberculosis (TB)) and therapeutic clinical research.
• Performs literature searches, attend meetings, etc. as needed to support regulatory document preparation, regulatory intelligence, and regulatory strategy, and to stay current with applicable therapeutic areas of clients.

Job Requirements

• Excellent oral and written communication skills; detail-oriented and able to multi-task/prioritize well.
• Ability to analyze medical research data and review experimental protocols.
• Strong working knowledge of Microsoft office; experience with SharePoint a plus.
• Professional or educational background in a scientific field, clinical trials, regulatory affairs or health care; familiarity with GCP and/or experience working in an FDA-regulated environment is desirable. General knowledge of the drug/vaccine development process or clinical trials is a plus.
• Experience in preparing regulatory documents, publishing regulatory submissions using electronic publishing software and proficiency in preparing documents that are compliant with electronic submission standards.
• This is a hybrid position with 2 days in TRI\'s Bethesda, Maryland office, and 3 days working remotely.

We are equal opportunity/affirmative action employers, committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status, or any other protected characteristic under state or local law.