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2+ years
Not Disclosed
10 Nov. 22, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Description

Katalyst HealthCares & Life Sciences Inc. is hiring entry-level candidates for several roles in contract research focused on clinical trials involving drugs, biologics, and medical devices. We collaborate with university hospitals, pharmaceutical companies, and recruiting partners to provide opportunities in Drug Safety, Pharmacovigilance, and Clinical Research.


Position Overview

Role: Medical Monitor
Job Type: Contract


Key Responsibilities

  • Provide medical leadership to regional monitoring staff.
  • Develop and maintain expertise in investigational compounds and their related therapeutic fields.
  • Oversee the safety of trial subjects during clinical studies.
  • Assist in the selection of Clinical Investigators for trials.
  • Manage Serious Adverse Event (SAE) reporting per established SOPs.
  • Ensure the timely distribution of IND reports to investigators and Ethics Committees (EC).
  • Review and approve study budgets in collaboration with clinical sites.
  • Analyze and review site monitoring reports to ensure participant safety.
  • Support CRAs in ensuring site compliance with GCP guidelines and company SOPs.
  • Exhibit strong communication skills to effectively liaise with stakeholders.

Additional Information

All candidate information will be kept confidential in accordance with EEO guidelines.