Associate Medical Director – Oncologist

Allucent

Directeur médical adjoint en oncologie supervisant la sécurité et l’intégrité des essais cliniques d’Allucent au Canada. Répondant aux questions de protocole, examinant les données et soutenant les équipes d’étude.

Posted 8/5/2026full-timeRemote • 🇨🇦 CanadaLead💰 CA$110,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in medical monitoring and oncology, ensuring compliance with GxP standards and applicable regulatory requirements. Capable of providing urgent medical support and training project teams on clinical trial protocols and safety issues.

Highest-signal resume keywords

Medical Degree (MD)Oncology ExpertiseGxP Standards KnowledgeRegulatory Compliance (GDPR/HIPAA, CFR/CTR/CTD)Excellent Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Medical MonitoringClinical Data ReviewProtocol InterpretationSAE ReviewRisk ManagementMedDRA CodingSafety Report AnalysisBudget TrackingTherapeutic Area TrainingProtocol Deviation Review

Soft Skills

Strong Administrative SkillsAbility to Work in Fast-Paced Environment

Tools & Technologies

WordExcelPowerPoint

Industry Keywords

Clinical TrialsMedical Monitoring PlansData Safety Monitoring BoardsClient Relationship ManagementTherapeutic and Drug Development Conferences

About the role

Key responsibilities & impact

Independently ensure the integrity and quality of the medical, clinical, and safety aspects of trials conducted by Allucent
Serve as the medical monitor contact for investigators and study site teams on protocol-related and participant safety questions
Provide medical monitoring support for assigned clinical studies: respond to medical queries, assist with protocol interpretation, and review clinical data
Assist the project manager in client discussions regarding safety issues or concerns
Prepare medical monitoring plans and other relevant plans prior to study initiation
Review serious adverse events (SAEs), SUSARs, and safety reports, and analyze similar events
Assist the clinical data management team with MedDRA and WHO coding
Review clinical study documents, including protocols, informed consent forms, clinical study reports, and safety reports
Contribute to the setup and conduct of data safety monitoring boards and dose-escalation meetings
Participate in study start-up meetings, investigator meetings, and other relevant meetings, and deliver presentations as required
Provide urgent medical support on a 24/7 basis
Train project teams on the medical aspects of trials and provide therapeutic area training
Review protocol deviations
Identify study-related risks and contribute to risk management plans
Review medical deliverables, contribute to budget tracking, and attend therapeutic and drug development conferences
Maintain client relationships and participate in client assessments, visits, and proposal presentations

Requirements

What you’ll need

Medical degree (MD)
Experience as an oncologist
At least three years of relevant professional experience with solid expertise in oncology
Good knowledge of GxP standards
In good standing with local, provincial, and national regulatory and licensing authorities, and with certification bodies
Knowledge of applicable regulatory requirements, including GDPR/HIPAA, CFR/CTR/CTD
Excellent written and verbal communication skills
Strong command of English
Ability to work in the fast-paced environment of a growing company
Strong administrative skills
Proficient in Word, Excel, and PowerPoint

Benefits

Comp & perks

Comprehensive benefits package based on workplace location
Competitive salaries depending on location
Departmental training and education budget to support professional development
Flexible working hours (where reasonably practicable)
Remote or hybrid work options depending on location
Opportunities to move into leadership positions and access to mentoring
Participation in our buddy program, available to new hires and existing employees
Internal mobility and career advancement opportunities
Employee referral program with financial incentives
Access to online training for soft and technical skills via ADP and our internal platforms
Eligibility for our spot bonus program, which rewards exceptional project contributions
Eligibility for our loyalty rewards program, recognizing long-term service and commitment