Glaukos

Clinical Project Manager/Sr. Project Manager

Glaukos$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required
  • 5+ years in project management within clinical research or relevant medical fields
  • Experience managing clinical studies from strategy to execution
  • Proficient in facilitating cross-functional team meetings
  • Strong organizational and analytical skills in managing multiple studies
  • Knowledge of pharmaceutical clinical study development and regulatory processes
  • Ability to thrive in an innovative and ambiguous setting

Responsibilities

  • Support the development of project plans, timelines, and resource allocation for clinical trials
  • Facilitate strategic cross-functional discussions for comprehensive clinical development
  • Collaborate with teams to align clinical project objectives with corporate goals
  • Create and maintain clinical study metrics for decision-making and bottleneck identification
  • Identify project risks and develop proactive mitigation strategies
  • Communicate project status, plans, and risks to stakeholders effectively
  • Proactively identify constraints and coordinate solutions with R&D management

Benefits

  • Opportunity to work on innovative pharmaceutical and medical device projects
  • Collaborative work environment with cross-functional teams
  • Engagement with strategic discussions at multiple organizational levels
  • Potential for personal development through training and implementation of project management best practices
  • Contributing to the adaptation and enhancement of project management processes and tools
Full Job Description
Job Description

What You'll Do:

The ClinicalProject Manager / Senior Project Manager is part of this group and will be working closely with the Clinical Development and Clinical Operation's teams, ensuring seamless coordination, integrated project plans and implementation of those project plans to meet defined objectives.

Key accountabilities include oversight of integrated project timelines, establishing and maintaining clinical study metrics to aid strategy development and decision making.
  • Support clinical teams with the development of project plans, timelines, and resource allocation for clinical trials and related activities
  • Facilitate cross functional strategic discussions to ensure all elements of applicable project development are planned and executed
  • Collaborate with cross-functional teams to ensure alignment with organizational goals.
  • Create and maintain clinical studies metrics that will aid decision making and identify bottlenecks
  • Helps to identify and manage risks, assisting in the development of proactive mitigation strategies
  • Communicate transparently and in a concise fashion to relevant stakeholders regarding clinical study status, plans, risks and strategy
  • Exercise excellent judgment in determining appropriate project communications to internal and external stakeholders
  • Proactively identifies critical path constraints and works with R&D management to identify solutions
  • Promote implementation and cross functional adoption of "fit for purpose" PMO tools, including MS Project, consistent use of SharePoint, and reporting and analytics tools
  • Promote implementation and cross functional adoption of project management best practices and assist with training and development supporting the implementation of the organization's PMO
  • Contribute to the development and refinement of project management processes, tools, and best practices within the clinical development and operations teams

    How You'll Get There:
  • Bachelor's Degree Required
  • 5 plus years of Clinical project management experience in medical device or pharmaceutical industries.
  • Knowledge of pharmaceutical and/or medical device development processes and deliverables at each stage of the pipeline, from early development to commercialization
  • Any clinical research or clinical operations experience would be preferable but not required.
  • Ability to work cross functionally and collaboratively to develop and execute development plans. Effective communication skills including written and verbal
  • Experience facilitating cross-functional team meetings to enable communication, decision-making, and alignment with internal and external stakeholders while managing project scope, deliverables, risks, and resources
  • Strong organizational, analytical, and problem-solving skills, including attention to detail
  • Comfort working in an innovative and entrepreneurial environment; operates well with ambiguity and proactively identifies and actions solutions
  • Adaptability to shifting strategies or changing project priorities
  • Experience in project management tools including Microsoft Project, Excel, SharePoint and PowerPoint; Advanced knowledge of analytical tools preferred

#GKOSUS

About Glaukos

Glaukos Corporation is an ophthalmic medical technology and pharmaceutical company focused on novel therapies for the treatment of glaucoma, corneal disorders and retinal diseases. The company pioneered Micro-Invasive Glaucoma Surgery, or MIGS, to revolutionize the traditional glaucoma treatment and management paradigm. Glaukos launched the iStent, its first MIGS device, in the United States in 2012 and is leveraging its platform technology to build a comprehensive and proprietary portfolio of micro-scale injectable therapies designed to address the complete range of glaucoma disease states and progression. The company's second-generation MIGS device, the iStent inject, was approved by the FDA in June 2018. Glaukos is also developing a pipeline of innovative technologies in corneal health, including the recently acquired Microline surgical platform, as well as novel drug delivery technologies.
Learn more about Glaukos
Size
727 employees
Market Cap
$1.9 billion
Industry
Net Income
-$120.3 million
Founded
1998
5 Year Trend
+20.8%
Revenue
$224.9 million
NASDAQ

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