bluedoor data·Job Postings API·bluedoor.sh ↗

HomeCompaniesAllucentVP Regulatory Affairs

VP Regulatory Affairs

Allucent · Cary, United States (Remote) · Remote · Deleted · Workable

Job facts

FieldValue
CompanyAllucent
TitleVP Regulatory Affairs
Normalized title-
Department / teamRegulatory Affairs
LocationCary, United States
Work modelRemote / Remote
Employment typeFull Time
Salary-
Statusdeleted
ATS providerWorkable
Posted / first seen2026-03-13 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-04

Related slices

PageWhat it containsOpen
Company jobsActive postings from Allucent.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Workable.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Cary.Open
Department jobsActive postings in Regulatory Affairs.Open
Work model jobsActive Remote postings.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

CompanyAllucent
Source67df5859-3537-4170-8b05-a728178eca42
ATS providerWorkable

Description

Description At Allucent™ , we are dedicated to helping small medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life changing therapies to patients in need across the globe. We are looking for a Vice President of Regulatory Affairs to join our A team (hybrid\ /remote). As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory Affairs, you will: Lead regulatory activities and team management : Assist clients with regulatory aspects of drug, biologic, or medical device products; provide counsel, manage the regulatory team (potentially with direct reports), and translate requirements into practical plans while ensuring timely, scientifically valid submissions. Oversee HA interactions and project leadership : Lead/participate in Health Authority communications (e.g., meetings, teleconferences); review/author regulatory content for submissions; contribute expertise on drug/device development as a Leadership team member reporting to Senior Leadership, serving on project teams in roles like Subject Matter Expert or Project Lead. This role is open to considering candidates from United States and Canada. Requirements B.Sc., M.Sc., Ph.D., or equivalent degree, in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development Advanced regulatory knowledge of drug, biologic, or device development focusing on regulatory requirements for US, EU/UK, and Canada RAC credentials preferred Skills: Critical thinking and analytical skills, financial acumen, influencing and leading teams, risk assessment, problem solving skills, decision making, strong written and verbal communication skills in English Strong computer skills, including SharePoint, Word, Excel, and PowerPoint Quality focus Strong emotional intelligence, customer focused leadership and decision making skills · Innovative, creative, and practical thinking including problem solving skills. Benefits Benefits of working at Allucent include: Comprehensive benefits package per location Competitive salaries per location Departmental Study/Training Budget for furthering professional development Flexible Working hours (within reason) Opportunity for remote/hybrid\ working depending on location Leadership and mentoring opportunities Participation in our Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Disclaimers: \ Our office based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices. “The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.” LI Remote LI Hybrid LI TCW

Full job record

Job ID622730df93835d4723dbba044270da65e7366046
Org IDddc65ac6-040f-49e3-b37c-08416cfd3b0b
Source ID67df5859-3537-4170-8b05-a728178eca42
Board ID67df5859-3537-4170-8b05-a728178eca42
Providerworkable
Provider Job Key44ECE24809
TitleVP Regulatory Affairs
Normalized Title
Statusdeleted
Activeno
Location TextCary, United States (Remote)
DepartmentRegulatory Affairs
Team
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
Region
CityCary
Salary RawDescription At Allucent™ , we are dedicated to helping small medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life changing therapies to patients in need across the globe. We are looking for a Vice President of Regulatory Affairs to join our A team (hybrid\ /remote). As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product. About the role As the VP Regulatory Affairs, you will: Lead regulatory activities and team management : Assist clients with regulatory aspects of drug, biologic, or medical device products; provide counsel, manage the regulatory team (potentially with direct reports), and translate requirements into practical plans while ensuring timely, scientifically valid submissions. Oversee HA interactions and project leadership : Lead/participate in Health Authority communications (e.g., meetings, teleconferences); review/author regulatory content for submissions; contribute expertise on drug/device development as a Leadership team member reporting to Senior Leadership, serving on project teams in roles like Subject Matter Expert or Project Lead. This role is open to considering candidates from United States and Canada. Requirements B.Sc., M.Sc., Ph.D., or equivalent degree, in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development Advanced regulatory knowledge of drug, biologic, or device development focusing on regulatory requirements for US, EU/UK, and Canada RAC credentials preferred Skills: Critical thinking and analytical skills, financial acumen, influencing and leading teams, risk assessment, problem solving skills, decision making, strong written and verbal communication skills in English Strong computer skills, including SharePoint, Word, Excel, and PowerPoint Quality focus Strong emotional intelligence, customer focused leadership and decision making skills · Innovative, creative, and practical thinking including problem solving skills. Benefits Benefits of working at Allucent include: Comprehensive benefits package per location Competitive salaries per location Departmental Study/Training Budget for furthering professional development Flexible Working hours (within reason) Opportunity for remote/hybrid\ working depending on location Leadership and mentoring opportunities Participation in our Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Disclaimers: \ Our office based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices. “The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.” LI Remote LI Hybrid LI TCW
Salary Min
Salary Max
Salary Currency
Salary Periodweek
Source URLhttps://apply.workable.com/allucent/jobs/view/44ECE24809
Apply URLhttps://apply.workable.com/allucent/j/44ECE24809/apply
First Seen At2026-05-31 17:47:36Z
Last Seen At2026-06-04 10:10:18Z
Last Checked At2026-06-06 13:32:22Z
Last Changed At2026-06-06 13:32:22Z
Inactive At2026-06-06 13:32:22Z
Source Posted At2026-03-13 00:00:00Z
Source Updated At
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=workable/board=allucent/date=2026-06-04/2026-06-04T10-10-17-761Z-118c9c187769583092f842b9a25718c0d5a32fbf3e25f6380151e18fb6be8dc0.json
Event Fields
{
  "content_hash": "5d7211e575b31c73f044f49e50e21a341fa28af4f0dabafee4c306b47e67f625",
  "source_hash": "3a767ca2d90deef064538a67c2ba77f1dad711e27adc6ed3a755d1debd887eb7",
  "last_changed_at": "2026-06-06T13:32:22.400Z",
  "active_status": "deleted"
}
Parsed Structured
{
  "language": "en",
  "location": {
    "raw": "Cary, United States (Remote)",
    "city": "Cary",
    "region": null,
    "country": "United States",
    "is_remote": true,
    "confidence": 0.95
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-04T10:10:18.478Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Cary, United States (Remote)",
      "city": "Cary",
      "region": null,
      "country": "United States",
      "is_remote": true,
      "confidence": 0.95
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": "remote",
  "salary_period": "week",
  "workplace_type": "remote",
  "salary_currency": null
}
Extensions
{}
Native Structured
{
  "detail": {
    "type": "Full-time",
    "title": "VP Regulatory Affairs",
    "posted": "2026-03-13",
    "company": "Allucent",
    "applyUrl": "https://apply.workable.com/allucent/j/44ECE24809/apply",
    "location": "Cary, United States (Remote)",
    "workplace": "remote",
    "department": "Regulatory Affairs",
    "descriptionText": "Description\n\nAt Allucent™ , we are dedicated to helping small medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life changing therapies to patients in need across the globe.\n\nWe are looking for a Vice President of Regulatory Affairs to join our A team (hybrid\\ /remote). As a VP Regulatory Affairs at Allucent, you are responsible for assisting clients with the regulatory activities of drug, biologic or medical device product.\n\n About the role \n\nAs the VP Regulatory Affairs, you will:\n\n Lead regulatory activities and team management : Assist clients with regulatory aspects of drug, biologic, or medical device products; provide counsel, manage the regulatory team (potentially with direct reports), and translate requirements into practical plans while ensuring timely, scientifically valid submissions.\n Oversee HA interactions and project leadership : Lead/participate in Health Authority communications (e.g., meetings, teleconferences); review/author regulatory content for submissions; contribute expertise on drug/device development as a Leadership team member reporting to Senior Leadership, serving on project teams in roles like Subject Matter Expert or Project Lead.\n\nThis role is open to considering candidates from United States and Canada.\n\n Requirements\n\n B.Sc., M.Sc., Ph.D., or equivalent degree, in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development\n Advanced regulatory knowledge of drug, biologic, or device development focusing on regulatory requirements for US, EU/UK, and Canada\n RAC credentials preferred\n\nSkills:\n\n Critical thinking and analytical skills, financial acumen, influencing and leading teams, risk assessment, problem solving skills, decision making, strong written and verbal communication skills in English\n Strong computer skills, including SharePoint, Word, Excel, and PowerPoint\n Quality focus\n Strong emotional intelligence, customer focused leadership and decision making skills · Innovative, creative, and practical thinking including problem solving skills.\n\n Benefits\n\n Benefits of working at Allucent include: \n\n Comprehensive benefits package per location\n Competitive salaries per location\n Departmental Study/Training Budget for furthering professional development\n Flexible Working hours (within reason)\n Opportunity for remote/hybrid\\ working depending on location\n Leadership and mentoring opportunities\n Participation in our Buddy Program as a new or existing employee\n Internal growth opportunities and career progression\n Financially rewarding internal employee referral program\n\n Disclaimers: \n\n\\ Our office based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.\n\n “The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.” \n\n LI Remote LI Hybrid LI TCW"
  },
  "list_job": {
    "id": "44ECE24809",
    "type": "Full-time",
    "title": "VP Regulatory Affairs",
    "posted": "2026-03-13",
    "salary": null,
    "location": "Cary, United States (Remote)",
    "detailUrl": "https://apply.workable.com/allucent/jobs/view/44ECE24809.md",
    "department": "Regulatory Affairs"
  },
  "detail_meta": {
    "url": "https://apply.workable.com/allucent/jobs/view/44ECE24809.md",
    "http_status": 200,
    "content_type": "text/markdown; charset=utf-8",
    "response_bytes": 3901
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/622730df93835d4723dbba044270da65e7366046?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/ddc65ac6-040f-49e3-b37c-08416cfd3b0bJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/67df5859-3537-4170-8b05-a728178eca42JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/622730df93835d4723dbba044270da65e7366046/eventsJSON