Clinical Trial Support - Regulatory Affairs Administrator

Job Title Clinical Trial Support - Regulatory Affairs Administrator Agency Texas A M University Department Research Compliance Biosafety Programs Proposed Minimum Salary $9,500.00 monthly Job Location College Station, Texas Job Type Staff Job Description Our Commitment Texas A M University is committed to enriching the learning and working environment by promoting a culture that respects all perspectives, talents lived experiences. Embracing varying opinions and perspectives strengthens our core values which are: Respect, Excellence, Leadership, Loyalty, Integrity, and Selfless Service. Who We Are The Clinical Research Support Office within the Division of Research serves as a centralized administrative resource to support investigators throughout the life cycle of clinical research involving human participants. What We Want The Clinical Research Support Office is seeking a Regulatory Affairs Administrator to serve as a subject matter expert in clinical trial operations and related administrative functions. This individual will play a vital role in supporting the development of regulatory strategies, providing regulatory guidance, and preparing and submitting regulatory communications and documents. The ideal candidate will ensure compliance with regulatory standards and facilitate the approval process for clinical research. In this role, you will work closely with investigators, administrators, regulatory agencies, and internal and external groups that support clinical research throughout the project life cycle. What You Need To Know Salary: $114,000 - $125,000/annually ( Compensation will be commensurate to the selected hire’s experience). Cover Letter/Resume: A cover letter and resume are highly encouraged. You may upload these in the CV/Resume section. Qualifications Required Education and Experience: Bachelor’s degree in applicable fields or equivalent combination of education and experience . 6 years of experience in clinical trials, research, or compliance roles, including regulatory support, business/research operations, confidentiality and clinical trial agreements, cost coverage analyses, and handling grants, contracts, budgets, and billing. Public speaking, presentation, analytical, negotiating, and collaborative skills to interact effectively with a broad spectrum of constituents, including faculty members, students, high-level administrators, IRB staff and sponsor representatives. Comprehensive understanding of research contracts, clinical