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Flourish Research

Clinical trial optimization and operations efficiency

Regulatory Specialist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeWalnut Creek, CA, USA$25 - $27 /hr

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • Experience in clinical or biological research is required; the stated range is 0–3+ years.
  • Experience with Microsoft Office applications, including Outlook, Word, and Excel, a clinical trial management system (CTMS), eRegs/eDocs, and other internet-based platforms is required.
  • The candidate must be detail-oriented, organized, self-motivated, able to work independently and collaboratively, and able to stay on task and meet deadlines.
  • Strong written and verbal interpersonal communication skills are required.
  • The candidate must demonstrate ethical decision-making when interacting with patients, sponsors, institutional review board representatives, physicians, satellite-site staff, and other employees.
  • Critical thinking and problem-solving skills are required.
  • The candidate must be professional, have a strong work ethic, adapt to additional tasks, and collaborate across departments to solve problems.
  • The candidate must have strong computer skills, including Office 365.
  • The candidate must be able to sit for extended periods, work in a clinical or office environment and a call center environment with occasional distractions, work occasional evenings and weekends, lift 35 pounds and occasionally more, drive, and have daily access to an automobile.

Responsibilities

  • Prepare, maintain, and oversee research-related regulatory documents.
  • Coordinate initial regulatory document submissions to institutional review boards, sponsors, and state or federal regulatory offices as needed.
  • Compile study information and submit initial, continuing, and final reports to institutional review boards and/or sponsors.
  • Prepare submission forms and submit updated documents, including amendments, addendums, investigator brochures, safety information, FDA Form 1572s, and informed consent documents.
  • File and maintain required logs in appropriate regulatory repositories.
  • Assist with and manage the archiving of clinical trial documents and records.
  • Prepare for monitoring visits and audits.
  • Distribute, collect, process, and track essential site regulatory documents for ongoing studies, including updated investigator, pharmacist, and nursing CVs, licenses, GCP, IATA, and training certificates, as applicable, across paper and electronic files.
  • Maintain the confidentiality of study protocol information and protected health information.
  • Create accurate written documents and reports, such as cover letters, notes to file, and memos.
  • Perform duties safely, prudently, and in a time- and cost-effective manner in accordance with company policies.
  • Represent the company professionally and courteously when interacting with staff, sponsors, contract research organizations, institutional review boards, participants, clinical staff, contract personnel, and others.
  • Perform other duties assigned by management.
  • Assist with key departmental initiatives and process improvements.
  • Assist with training new company hires.
  • Meet at least 80% of annual goals.

Desired Qualifications

  • A college degree is preferred but not required.

About the Company

Flourish Research

Clinical trial optimization and operations efficiency

Flourish Research helps healthcare and pharmaceutical clients run clinical trials more efficiently. It offers tailored optimization services that improve trial operations, aiming to reduce time and costs to bring new treatments to market. The company leverages decades of experience to provide quality-driven solutions, focusing on expanding capabilities, developing healthy teams, and implementing processes that enhance speed and quality across trial activities. Flourish Research differentiates itself by its client-specific approaches and strong emphasis on quality, team development, and operational excellence to deliver reliable trial outcomes.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Apex, NC
Founded
2021

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