Medical Monitor, Canada Board-Certified Psychiatrist

🔥 0 minutes ago

🇨🇦 Canada – Remote

⏱ Part Time

🟠 Senior

🔴 Lead

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Act as the primary point of contact for trial-specific medical and safety-related questions • Provide input for responses to regulatory authorities and IRBs/IECs • Monitor trial participant safety • Participate in participant recruitment boost and retention activities • Present on medical matters at kick-off and investigator meetings • Train trial teams in the therapeutic area and medical aspects of protocols • Develop and review trial-specific documents within medical monitoring scope • Manage ongoing trial risks related to medical monitoring • Perform ongoing medical review of operational clinical trial databases • Review protocol deviations, RAE reports, SAE narratives, IND/SUSAR Safety Reports and annual IND reports • Support Pharmacovigilance, Medical Data Review and Data Management with safety and database reconciliation • Participate in trial-related committees such as IDMC and adjudication committees • Review clinical study reports, including safety narratives and TFLs • Provide medical expertise on an as-needed basis • Prepare for and participate in trial audits and follow up on audit findings • Participate in feasibility assessments of potential and ongoing trials in Canada/region • Participate in bid defense meetings and client interactions • Act as a medical expert and provide therapeutic expertise to other PSI departments

🎯 Requirements

• Medical Doctor degree required • Canada Board Certification in psychiatry required • Minimum of 10 years of experience as a practicing psychiatrist • Clinical Research experience preferred • Proficiency with MS Office applications • Communication, presentation and analytical skills • Problem-solving, team-oriented and detail-oriented • Based anywhere in Canada

🏖️ Benefits

• Part-time/consultant role • Remote work from anywhere in Canada • Opportunity to join PSI's international group of medical professionals • Career development on the frontline of medical science • Opportunity to use medical knowledge and expertise to help bring new medications to patients