
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
💰 $75M Private Equity Round on 2015-12
Healthcare • Consulting • Logistics
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
🔥 45 minutes ago
Where this job comes from
Posted on Precision For Medicine's careers page, not through a job board
First seen by Remote Rocketship 45 minutes ago
Still open on Precision For Medicine's site. Checked 31 minutes ago.

1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
💰 $75M Private Equity Round on 2015-12
Healthcare • Consulting • Logistics
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
• Lead new and existing CRO laboratory projects across assay development, clinical testing, biorepository/sample management and logistics, and kitting for client studies • Lead projects from conception through close-out, including planning, execution, risk management, communication, stakeholder management, scope and cost control • Manage designated protocols and remain accountable for project performance and client satisfaction throughout project lifecycles • Serve as cross-functional lead and monitor delivery against contracted timelines and budgets • Create and manage project timelines, budgets, revenue goals, forecasts, and resource plans • Coordinate and supervise scheduled activities and delegate responsibilities • Lead implementation of new and ongoing studies and coordinate new project development • Create, track, and report project timelines, metrics, and business measurements • Communicate with clients and collaborators regarding data management, inventory control, and shipping procedures • Prepare and present project information at internal and external meetings and prepare reports and correspondence • Evaluate budgets monthly, report unexpected variances, and meet assigned revenue and expense objectives • Identify out-of-scope work, escalate findings and action plans, and manage operational issues • Review and maintain project documentation to approvable status • Assess and mitigate technical, project, and business risks • Ensure deliverables comply with design, performance, regulatory, and client standards • Monitor assignments, adjust priorities and schedules, and deliver high-quality work • Provide internal project management consulting, identify process improvements, mentor junior Project Managers, and assist senior staff
• Bachelor's degree in a life science or related field plus a minimum of 5 years of project management experience in biotechnology, clinical trials, central lab, repository, or pharmaceutical industry; an equivalency consisting of appropriate education, training and/or directly related experience may be considered sufficient • Excellent computer skills and experience with MS Office/MS 365 applications • Proven coordination and communication with teams across R&D, Operations, Finance, Business Development, Sales, Manufacturing, Executive Management, Quality Assurance, and Regulatory Affairs • Ability to lead and drive stakeholder discussions • Excellent presentation, interpersonal, organizational, and multi-tasking skills • Strong emotional intelligence • Ability to work in front of a computer for long hours • Strong understanding of project management and data analysis • Strong critical thinking, analytical, and problem-solving skills • Exceptional judgment and discretion • Fluent English reading, writing, speaking, and comprehension • Proven ability to work proactively and productively as a team player • Valid driver's license • Ability to travel domestically and internationally, including overnight stays, approximately 10–25% • Ability to work extended hours when necessary • Familiarity with GCLP, GLP, GMP, CLIA, and ISO regulatory guidelines preferred • Familiarity with Smartsheet or other project management tools preferred • Must be legally authorized to work in the country of employment without employer sponsorship
• Employees are appreciated for their contributions • Employee input and ideas are valued and nurtured • Equal opportunity employment • Reasonable accommodation support for applicants with disabilities
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