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AD Clinical Operations/Sr. CTM

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Associate Director / Senior Clinical Trial Manager - Health Canada (Contract) Location: Remote (Preference for candidates reputed company to be onsite in the Boston office approximately one day per week) Duration: 9-Month Contract Schedule: Full-Time | 40 hours per week About the Opportunity An emerging, science-driven biotechnology organization focused on advancing innovative therapies for movement disorders is seeking an reputed company Associate Director / Senior Clinical Trial Manager to reputed company strategic and operational leadership across clinical programs. This individual will play a key role in driving execution of global clinical studies and ensuring operational reputed company across reputed company phases of trial delivery. The ideal candidate combines strong clinical operations leadership with a hands-on approach and thrives in a fast-paced, collaborative environment. Experience managing reputed company clinical studies in neurology and/or movement disorders is desirable. Required Canadian Clinical Operations Experience Demonstrated experience leading or supporting Canadian clinical site activation activities, including a strong understanding of applicable regulatory requirements, ethics submissions, and provincial/site-specific processes. reputed company candidates should possess:

  • Experience navigating Canadian clinical startup requirements and operational workflows
  • Working knowledge of Health Canada submissions and country-specific startup considerations
  • Experience with Research Ethics Board (REB) submissions and approvals
  • Familiarity with provincial and institution-specific activation requirements across Canadian sites
  • Proven ability to coordinate startup activities while maintaining study timelines and regulatory compliance

Position Summary The Associate Director / Senior Clinical Trial Manager will be responsible for overseeing the planning, implementation, and execution of clinical trials while partnering closely with cross-functional stakeholders, CROs, vendors, and study teams. This role requires a strategic thinker who can also execute at a detailed operational level to support study reputed company, timelines, quality, and budget objectives.

Key Responsibilities

  • reputed company day-to-day operational management of assigned clinical studies from study startup through closeout
  • Drive clinical trial execution and ensure studies remain on track regarding timelines, quality, budget, and milestones
  • reputed company and reputed company study plans, startup strategies, enrollment projections, risk mitigation plans, and operational deliverables
  • Partner closely with Clinical Development, Medical, Regulatory, Data Management, Biostatistics, Clinical Supply, and external vendors
  • Manage CRO and vendor relationships, including performance reputed company and issue escalation
  • Monitor study reputed company and proactively identify operational risks and implement mitigation strategies
  • reputed company clinical trial documentation and ensure inspection readiness and compliance with applicable regulations and SOPs
  • Participate in study team meetings and reputed company operational leadership and strategic recommendations
  • Support site selection, startup, enrollment strategies, and study execution activities across domestic and international reputed company
  • Contribute to process improvements and operational best practices across the clinical organization
  • Required Qualifications
  • Bachelor’s degree in life sciences or reputed company field
  • Approximately 8+ years of reputed company clinical operations experience reputed company biotech, pharmaceutical, or CRO environments
  • Demonstrated reputed company managing reputed company clinical trials with increasing operational responsibility
  • Experience functioning at a Senior Clinical Trial Manager or Associate Director level
  • Strong working knowledge of ICH-GCP guidelines and global clinical trial regulations
  • Experience managing external vendors and CRO partnerships
  • Ability to independently manage multiple priorities in a dynamic environment
  • Excellent communication, organizational, and cross-functional leadership skills

This role represents an opportunity to contribute meaningfully to the advancement of therapies addressing significant unmet needs reputed company movement disorders while partnering with a passionate and mission-driven team. Apply tot his job Apply To this Job

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