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Healthcare, Oncology

Regulatory Affairs Associate - Full Time - Germantown, TN

Germantown, TNOnsiteFull TimePosted 16 days agoVisa sponsorship available

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Required skills

  • Regulatory Affairs Associate
  • IRB submissions
  • regulatory documentation
  • safety reports
  • federal regulations
  • GCP
  • Sponsors
  • CROs
  • investigators
  • research staff

Nice to have

  • Associate's degree

Role summary

West Cancer Center is seeking a Regulatory Affairs Associate I to coordinate regulatory submissions and approvals for clinical research studies. This role involves managing IRB submissions, maintaining regulatory documentation, processing safety reports, and ensuring compliance with federal regulations. The associate will work closely with sponsors, CROs, investigators, and research staff, maintaining study binders and supporting audits. The position requires strong organizational and communication skills, familiarity with federal regulations and GCP, and proficiency in computer applications. This role offers a meaningful impact, collaborative culture, and professional development opportunities within a mission-driven environment.

Job Title: Regulatory Affairs Associate

About UsAt West Cancer Center, we are dedicated to providing compassionate, patient-centered care while advancing groundbreaking research. Our team fosters collaboration, innovation, and professional growth, ensuring that every role contributes to making a difference in patients’ lives. Join us in our mission to provide comprehensive support to those navigating the challenges of cancer treatment.

Position OverviewThe Regulatory Affairs Associate I works closely with Sponsors, CROs, investigators, and research staff to coordinate regulatory submissions and approvals for multiple studies. This role is responsible for managing Institutional Review Board (IRB) submissions, maintaining regulatory documentation, processing safety reports, and ensuring compliance with federal regulations while supporting ongoing research activities.

Key Responsibilities

  • Coordinate initial and ongoing IRB approvals for assigned studies
  • Maintain regulatory responsibility for multiple studies
  • Collect and maintain site-specific regulatory documents (CVs, licenses, lab certifications, FDA Form 1572, delegation logs, etc.)
  • Prepare and submit study documents to IRB, Sponsors, and/or FDA as appropriate
  • Maintain study binders with required documents and correspondence
  • Meet study deadlines and coordinate with staff for subject information needed for updates and re-approvals
  • Perform study closeout activities as appropriate
  • Maintain essential regulatory documents
  • Obtain IRB approval for updated study documents (protocol amendments, informed consent forms, Investigator Brochures, patient materials, etc.)
  • Manage site changes including regulatory updates and documentation
  • Process safety reports
  • Maintain working knowledge of federal regulations
  • Participate in Sponsor/CRO monitoring visits and audits
  • Assist with report compilation, quality control of regulatory documents, and other assigned tasks
  • Maintain professionalism and confidentiality in all interactions
  • Assist with training and orientation of new employees
  • Interface with external partners including sites, sponsors, CROs, IRBs, and FDA
  • Perform all other duties as assigned

    • Qualifications

    Education & ExperienceRequired:

  • Two (2) years of regulatory affairs or research experience

    • Preferred:

  • Associate’s or Bachelor’s degree
  • Research certification

    • Skills & Abilities

  • Strong organization and follow-up skills
  • Excellent verbal and written communication skills
  • Familiarity with Code of Federal Regulations and Good Clinical Practice (GCP)
  • Strong problem-solving skills
  • Ability to organize and prioritize work assignments
  • Ability to manage multiple priorities in a fast-paced environment
  • Ability to analyze situations and respond in a timely manner
  • Ability to work in multi-functional teams
  • Proficiency in computer applications including Word, Excel, Adobe Acrobat, email, and internet research

    • Why West Cancer Center is a Great Place to Work

  • Meaningful Impact: Play a direct role in supporting patients through one of the most challenging times of their lives.
  • Collaborative Culture: Work alongside a multidisciplinary team of dedicated professionals committed to improving cancer care.
  • Professional Development: Benefit from ongoing training, educational resources, and growth opportunities.
  • Mission-Driven Environment: Be part of an organization guided by compassion, integrity, and innovation.

    • No nights, weekends, or holidays. Comprehensive benefits package.

    Join UsIf you are detail-oriented and passionate about supporting clinical research and regulatory compliance, we invite you to join West Cancer Center as a Regulatory Affairs Associate I and contribute to advancing innovative cancer care.

    Ready to apply?
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