Clinical Research Scientist

SmartRecruiters, Inc.

Madison (NJ)

Sur place

USD 68 000 - 97 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Competitive pay

Résumé du poste

Global Channel Management in New Jersey seeks professionals with advanced degrees and industry experience in clinical development and trial management to support regulatory submissions and BE studies. Candidates should have familiarity with regulatory dossiers, drug development processes, and GCP/ICH/FDA guidelines.

Roles emphasize experience with clinical trial management in university, hospital, or CRO settings and readiness to contribute to cross-functional teams in a fast-paced environment.

Qualifications

  • Experience in writing clinical portions of regulatory dossiers highly preferred
  • Knowledge of drug development (all clinical research process including protocol and case report form design, etc)
  • Knowledge of GCP/ICH guidelines and FDA regulations

Formation

MD/PhD/PharmD
MS
BS

Description du poste

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications
  • MD, PhD, or PharmD: 0 to 3 years with industry experience in clinical development and bioequivalence (BE) clinical trial management or similar experience in university, hospital or research organization
  • MS: 3 to 5 years of clinical development/clinical trial management
  • BS: 5 to 8 years with industrial or CRO clinical experience
  • Experience in writing clinical portions of regulatory dossiers highly preferred
  • Knowledge of drug development (all clinical research process including protocol and case report form design, etc)
  • Knowledge of GCP/ICH guidelines and FDA regulations
Additional Information

$60/hr

12 MONTHS

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