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Clinical Trials Regulatory Specialist 2 (Remote Opportunity)

Stanford University

United States · HybridJobSeen 2w agoSeen in employer's feed 2 days ago

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At a glance

Compensation
No compensation found
Location
United StatesHybrid
Work Authorization
Not specified

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Job overview

The Clinical Trials Regulatory Specialist 2 will work within Stanford's Clinical Research Hub, collaborating with clinical operations, finance, quality assurance, education, and business development teams to ensure compliance with Good Clinical Practices and Standard Operating Procedures while engaging sponsors, IRBs, the FDA, and other regulatory bodies.

Skills & qualifications

RequiredNice to have

Skills

Regulatory SubmissionsGood Clinical PracticesStandard Operating ProceduresInterpersonal SkillsCommunicationDiplomacyProject Management

Qualifications

Regulatory Submissions Experience

Full job description

Job Description

The Clinical Research Hub (CRH) (https://domcrh.stanford.edu/) is part of the Stanford Department of Medicine. CRH is seeking a mission-driven Clinical Trials Regulatory Specialist 2. In this role, you will collaborate with a high-performing team of clinical operations staff and medical experts. Your responsibilities will include ensuring compliance with Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs), while working closely with clinical operations, finance, quality assurance, education, and business development managers. You will engage with company sponsors, clinical research organizations, Stanford investigators and their study teams, the Stanford Institutional Review Board (IRB), other external IRBs, the FDA, and various regulatory authorities, as well as any other entities that contribute to clinical research at our institution.

The ideal candidate will possess exceptional interpersonal, communication, and diplomacy skills, along with the ability to manage multiple projects effectively. Previous experience in regulatory submissions and direct collaboration with clinical experts and industry sponsors is required. A strong commitment to integrity, excellence, and continuous improvement is essential. This position offers flexibility in work arrangements, including onsite, hybrid, or remote options.

At CRH, we are dedicated to finding team members who are passionate about their work, adaptable, and enthusiastic about achieving results. We prioritize equipping our staff to perform their roles efficiently, facilitating skill development and opportunities for growth within the organization. We support our team in maintaining a healthy work-life balance and encourage applicants who want to make a significant impact through global-reaching clinical research to apply!

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