Alcon

Clinical Project Manager

Alcon$100K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in a scientific, healthcare or related discipline
  • Experience leading clinical studies or complex clinical research projects
  • Strong understanding of the clinical drug development process
  • Proven ability to lead and influence cross-functional teams
  • Knowledge of Good Clinical Practice and clinical research regulations
  • Excellent communication and stakeholder management skills

Responsibilities

  • Lead end-to-end delivery of clinical studies from initiation to close-out
  • Drive study execution, tracking progress and managing risks
  • Partner with global and local teams for recruitment and data delivery
  • Chair study team meetings as primary operational contact
  • Monitor study performance and resolve operational challenges
  • Champion compliance and quality standards throughout the trial lifecycle
  • Support continuous improvement initiatives and inspection readiness

Benefits

  • Hybrid working model (Montreal and Toronto)
  • Opportunity to lead transformative clinical studies
  • Collaborative work environment across diverse teams
  • Engage in quality and compliance-focused projects
  • Potential to impact patient outcomes through innovative medicines
Full Job Description

Job Description Summary

#LI-Hybrid

Location: Montreal, Canada
Additional Location: Toronto, Canada

Relocation Support: This role is based in Toronto, Canada. Novartis is unable to offer relocation support: please only apply if accessible.

Imagine leading clinical studies that have the potential to transform patient outcomes around the world. As a Clinical Project Manager at Novartis, you will play a pivotal role in the successful delivery of clinical trials, driving execution from site initiation through to study close-out. Working across diverse teams and geographies, you will coordinate study activities, manage risks, champion quality and compliance, and ensure key milestones are achieved. This is an exciting opportunity to combine project leadership, collaboration and operational excellence to help bring innovative medicines to patients faster.

Job Description

Key Responsibilities

  • Lead end-to-end delivery of clinical studies from site initiation through study close-out.

  • Drive study execution, tracking progress, timelines, risks and mitigation plans across assigned countries.

  • Partner with global and local teams to achieve recruitment, quality and data delivery goals.

  • Chair study team meetings and act as the primary operational contact for assigned studies.

  • Monitor study performance and resolve operational challenges to maintain delivery against commitments.

  • Champion compliance, patient safety and quality standards throughout the clinical trial lifecycle.

  • Support continuous improvement initiatives and inspection readiness activities across the study portfolio.

Essential Requirements

  • Degree in a scientific, healthcare or related discipline.

  • Experience leading clinical studies or complex clinical research projects.

  • Strong understanding of the clinical drug development process and study execution activities.

  • Proven ability to lead and influence cross-functional teams within a matrix environment.

  • Knowledge of Good Clinical Practice, ethical requirements and clinical research regulations.

  • Excellent communication, stakeholder management and problem-solving skills.

Skills Desired

About Alcon

Alcon is a global medical company specializing in eye care products and services. The company's products include surgical equipment, contact lenses, and eye drops. Alcon was founded in 1945 and is headquartered in Baar, Switzerland. The company operates in over 70 countries and has over 20,000 employees. In 2019, Alcon became an independent publicly traded company after being spun off from Novartis.
Learn more about Alcon
Size
24,389 employees
Market Cap
$33.3 billion
Industry
Founded
1945
NASDAQ

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