bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesWest Cancer CenterRegulatory Affairs Associate - Full Time - Germantown, TN

Regulatory Affairs Associate - Full Time - Germantown, TN

West Cancer Center · Germantown, TN · Active · Greenhouse

Job facts

FieldValue
CompanyWest Cancer Center
TitleRegulatory Affairs Associate - Full Time - Germantown, TN
Normalized title-
Department / teamResearch
LocationGermantown, TN, United States
Work model-
Employment type-
Salary-
Statusactive
ATS providerGreenhouse
Posted / first seen2026-06-01 / 2026-06-02
Changed / last seen2026-06-02 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from West Cancer Center.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Greenhouse.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Germantown.Open
Department jobsActive postings in Research.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyWest Cancer Center
Source7cd19eaf-d3f5-48d9-9b87-659d25275c0e
ATS providerGreenhouse

Description

Job Title: Regulatory Affairs Associate About Us At 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 Overview The 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 & Experience Required: 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 Us If 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.

Full job record

Job IDa72ca7cdb20d4d4174df4a35f51fb5b0a18c8f93
Org ID5f404ba6-0883-44d6-aec3-f42da177ee32
Source ID7cd19eaf-d3f5-48d9-9b87-659d25275c0e
Board ID7cd19eaf-d3f5-48d9-9b87-659d25275c0e
Providergreenhouse
Provider Job Key8573822002
TitleRegulatory Affairs Associate - Full Time - Germantown, TN
Normalized Title
Statusactive
Activeyes
Location TextGermantown, TN
DepartmentResearch
Team
Employment Type
Workplace Type
Remote Policy
CountryUnited States
RegionTN
CityGermantown
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://job-boards.greenhouse.io/westcancercenter/jobs/8573822002
Apply URLhttps://job-boards.greenhouse.io/westcancercenter/jobs/8573822002
First Seen At2026-06-02 12:10:21Z
Last Seen At2026-06-06 07:33:55Z
Last Checked At2026-06-06 07:33:55Z
Last Changed At2026-06-02 12:10:21Z
Inactive At
Source Posted At2026-06-01 19:39:27Z
Source Updated At2026-06-01 19:39:27Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=greenhouse/board=westcancercenter/date=2026-06-06/2026-06-06T07-33-55-652Z-7fc2bdfcb9e88b52d0bd0ccf91d3eaffb88b4fd971e9871f7095506ec6b40c8f.json
Event Fields
{
  "content_hash": "26038416db1a20813c6dbd14d8acb9397b89d0d83e20a207b274bd2d68773248",
  "source_hash": "e72f22191df4963e2767cc89afbbd161489c373d1a5f452085081bda3968a64e",
  "last_changed_at": "2026-06-02T12:10:21.713Z",
  "active_status": "active"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "Germantown, TN",
    "city": "Germantown",
    "region": "TN",
    "country": "United States",
    "is_remote": false,
    "confidence": 0.9
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-06T07:33:55.793Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Germantown, TN",
      "city": "Germantown",
      "region": "TN",
      "country": "United States",
      "is_remote": false,
      "confidence": 0.9
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": null,
  "salary_period": null,
  "workplace_type": null,
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "title": "Regulatory Affairs Associate - Full Time - Germantown, TN",
  "offices": [
    {
      "id": 4011353002,
      "name": "GVS",
      "location": "Germantown, Tennessee, United States",
      "child_ids": [],
      "parent_id": 4011342002
    }
  ],
  "language": "en",
  "location": {
    "name": "Germantown, TN"
  },
  "metadata": [],
  "updated_at": "2026-06-01T15:39:27-04:00",
  "departments": [
    {
      "id": 4092514002,
      "name": "Research",
      "child_ids": [],
      "parent_id": null
    }
  ],
  "company_name": "West Cancer Center",
  "requisition_id": 6405801002,
  "first_published": "2026-06-01T15:39:27-04:00",
  "application_deadline": null
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/a72ca7cdb20d4d4174df4a35f51fb5b0a18c8f93?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/5f404ba6-0883-44d6-aec3-f42da177ee32JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/7cd19eaf-d3f5-48d9-9b87-659d25275c0eJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/a72ca7cdb20d4d4174df4a35f51fb5b0a18c8f93/eventsJSON