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Première détection par notre source: il y a 25 jours

Regulatory Affairs Consultant - Fully Remote | Upto $170/hr

@ Mercor

Toutes ses offres Site Web

Toronto, Ontario

130–170 $/h5+ ans d’expérience
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En bref

Mercor is hiring a remote contract Clinical Regulatory Expert at $130 to $170 per hour, for 20 to 25 hours a week. The role validates clinical data rooms and documents against FDA standards, and authors FDA information requests and model responses to help train AI systems. Candidates need 5+ years in regulatory roles and an MD, PhD, PharmD or equivalent.

Salaire :

130 $–170 $ de l’heure

Responsabilités :

  • Validate clinical data rooms and documents against FDA standards
  • Author FDA information requests and model responses
  • Design prompts, golden outputs and rubrics for AI agents
  • Test for deliberate defects and regulatory judgment

Résumé des exigences :

  • 5+ years of experience in regulatory roles
  • MD, PhD, PharmD or equivalent
  • Experience with FDA information requests across CMC, patient-level data, investigator qualifications and endpoint evidence
  • No conflict of interest with a current federal employer

Outils et compétences

Regulatory affairsResearchRegulatory complianceWork independentlyMeet deadlines
Source et dates

Type de source non vérifié · manatal

Date publiée par l’employeur
Non fourni
Première détection par notre source
2026-10-17
Mise à jour du dossier source
2026-10-17

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauSenior
DomaineMédecins et pratique avancée
Expérience5 an(s) et plus
Heures par semaine22.5
Déplacementsavion : aucun · route : aucun
Milieu de travailDomicile
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
FormationDoctorat (exigé)

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Postuler

Mercor

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

We connect human expertise with leading AI labs and enterprises to train frontier models.

Description complète de l’entreprise

Mercor is defining the future of work. We connect human expertise with leading AI labs and enterprises to train frontier models.

Abonnés LinkedIn
654 507
Personnes associées sur LinkedIn
5 250
Bureaux déclarés
  • San Francisco, California 94105, US
Catégories d’activité
  • Employment
  • Software
  • Recruiting
  • Data Collection and Labeling
  • Artificial Intelligence (AI)
  • Machine Learning
Autres noms enregistrés
  • Mercor
Le profil indique une agence de recrutement
Oui
Investissement total déclaré
483 600 000

La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.

Toutes ses offres Site Web

Mercor is defining the future of work. We connect human expertise with leading AI labs and enterprises to train frontier models.

ChampValeur
SecteurSoftware Development
Taille51-200 employees
Siège socialSan Francisco, California
Type d’organisationPrivately Held
Fondée en2023
Offres sur Jobsy1 626
LinkedInVoir la page
Description

About the job

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey.

Position: Clinical Regulatory Expert
Type: Contract
Compensation: $130–$170/hour
Location: Remote
Commitment: 20–25 hours/week

Role Responsibilities

  • Validate clinical data rooms and documents against FDA evidentiary standards and formatting expectations.
  • Author FDA information requests and model responses. Design prompts, golden outputs, and rubrics to quantify AI agent capabilities.
  • Ensure compliance with deliberate defects testing regulatory judgment.
  • Work independently and asynchronously to meet deadlines and improve AI model performance.

Qualifications

Must-Have

  • 5+ years of experience in regulatory roles.
  • MD, PhD, PharmD, or equivalent.
  • Experience reviewing or responding to FDA information requests across CMC, patient-level data, investigator qualifications, and biomarker or endpoint evidence.
  • No conflict of interest with a current federal employer.

Preferred

  • 10–25 years of experience.
  • Direct FDA review experience preferred over sponsor-side liaison work.

Application Process (Takes 20–30 mins to complete)

  • Upload resume
  • AI interview based on your resume
  • Submit form

Resources & Support

  • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome
  • For any help or support, reach out to: [email protected]

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

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