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Medical Monitor

5+ years
Not Disclosed
10 Jan. 30, 2025
Job Description
Job Type: Full Time Education: MD 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

🌟 Now Hiring: Medical Monitor (Canada) 🌟

πŸ’Ό Position: Medical Monitor
🏒 Industry: CRO - Medical Affairs
πŸ“ Location: Canada (Remote or Montreal HQ)
⏳ Job Type: Full-time

πŸ”Ž Job Overview

As a Medical Monitor, you will provide crucial medical and scientific support to clinical research programs, ensuring the integrity and safety of study protocols. This role is ideal for someone who is adept at building positive relationships with stakeholders, navigating the complexities of clinical trials, and interpreting large volumes of data to provide expert guidance.

πŸ”‘ Key Responsibilities

βœ” Protocols and Projects

  • Stay current on study protocols, amendments, and relevant clinical research guidelines
  • Develop or review medical monitoring plans and safety reporting plans
  • Provide project team training on study protocols and therapeutic areas
  • Prepare for and attend Investigators’ Meetings
  • Participate in business development activities (bid defense)

βœ” Medical Dermatology Advisory Role

  • Provide 24/7 on-call service for urgent safety issues and protocol questions
  • Offer first-line contact for investigators, site personnel, and monitors on study-related medical/safety issues
  • Assess the impact of prohibited medications and advise on appropriate action
  • Evaluate subject dropout replacements
  • Act as a subject matter expert on medical dermatology for internal and external stakeholders

βœ” Data Activities

  • Review safety-related data listings to identify trends and safety concerns
  • Ensure accurate medical reporting of adverse events (AEs) and serious adverse events (SAEs)
  • Review laboratory alerts and coordinate appropriate follow-up
  • Escalate safety or data integrity concerns to the Project Manager or Sponsor

βœ” Safety Monitoring & Reporting

  • Verify medical accuracy of subject safety data
  • Conduct emergency unblinding of randomized treatment assignments, if applicable

πŸ“Œ Requirements

πŸŽ“ Education:

  • Medical degree (MD)
  • Candidates with medical education and training completed outside of Canada are encouraged to apply
  • This position does not require a permit to practice medicine (non-practicing physician role)

πŸ›  Experience:

  • Minimum 5 years of clinical research experience in a CRO, pharmaceutical, or biopharmaceutical company
  • Proven ability to work effectively within a multidisciplinary team and adapt to shifting priorities

πŸ“œ Knowledge & Skills:

  • Excellent oral and written English communication skills (additional languages are a plus)
  • Strong problem-solving, organizational, and interpersonal skills

🎯 Perks & Benefits

✨ Permanent full-time position
✨ Flexible work schedule
✨ Comprehensive benefits: medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities
✨ Ongoing learning and development
✨ Option to work remotely or from our Montreal headquarters (depending on company policies and public health directives)

πŸ“Œ Company: Innovaderm (Specialized in Dermatology CRO Research)
πŸ“Œ Legal Requirement: Applicants must be legally eligible to work in Canada

πŸ“© Apply Now!