Bayside Solutions

Manager, Clinical Regulatory Affairs

in Redwood City, California

New Job

Job Description Job Attributes+

  • Req ID

    24026_1760488715

  • Job Category

    Science and Research

  • Job Type

    Contract

  • Hourly Salary

    From $0 to $0

  • Job Location

    Redwood City, California
    United States

Overview

Manager, Clinical Regulatory Affairs

W2 Contract-to-Hire

Salary Range: $208,000 - $270,400 per year

Location: Redwood City, CA - Hybrid Role

Job Summary:

The Manager of Regulatory Affairs will provide project teams with regulatory advice, manage and coordinate various Regulatory Affairs activities within and between departments, and obtain and maintain National Health Authority approvals for investigational products. The position may also undertake regulatory intelligence and research supporting company decision-making.

Duties and Responsibilities:

  • Manage planning, preparation, coordination, and submission of regulatory documents to global National Health Authorities. Such submissions may include Clinical, Preclinical, or CMC content.
  • Correspond and collaborate with colleagues and departments to achieve alignment.
  • Function as a Regulatory Affairs subject matter expert member of cross-functional teams, including study teams and submission teams.
  • Perform regulatory research to inform business strategy. Assess and communicate risks.
  • Assure that there are no significant interruptions to the business due to regulatory compliance issues.
  • Collaborates across the organization at all levels, functional groups, and with executive management.
  • Develop regulatory strategies to inform associated budgets, tools, and specialized support necessary for efficient operations.

Requirements and Qualifications:

  • Bachelor's Degree in a relevant field and at least 3 years of direct Regulatory experience.
  • Strong working knowledge of US FDA Pharmaceutical regulations and guidance.
  • Proven track record of successful submissions within a regulatory environment.
  • Exceptionally strong team player with excellent interpersonal and communication skills.
  • Detail-oriented with strong organizational skills and high-quality standards.

Preferred Qualifications:

  • Knowledge of EU EMA Pharmaceutical regulations and guidance preferred.
  • Direct experience with IND/NDA filings.

Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.

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