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Project Manager – Global Project Management, Lab Services

🔥 3 minutes ago

🇸🇬 Singapore – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

Where this job comes from

Posted on Precision Medicine Group's careers page, not through a job board

First seen by Remote Rocketship 3 minutes ago

Logo of Precision Medicine Group

Precision Medicine Group

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Lead new and existing CRO laboratory projects across assay development and 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 control, and cost control • Manage designated protocols and overall project performance and client satisfaction • 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 as the client-facing company representative • Coordinate development and implementation of new projects • Communicate with clients and collaborators regarding data management, inventory control, and shipping procedures • Coordinate data gathering and prepare/present project information, reports, and correspondence • Track project metrics, revenue objectives, expenses, budgets, and variances • Identify out-of-scope work and escalate findings and action plans • Review and update project documentation to approvable status • Assess and mitigate technical, project, and business risks • Ensure work complies with design and performance standards, regulatory requirements, and client expectations • Identify and resolve operational issues • Mentor junior Project Managers and provide internal project management consulting • Adjust priorities and schedules to meet deadlines and complete additional project, client, and departmental tasks

🎯 Requirements

• 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 combining appropriate education, training and/or directly related experience may be considered • Excellent computer skills and experience with MS Office/MS 365 applications • Proven coordination and communication with team members 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 • Skilled emotional intelligence • Able 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 • Able to read, write, fluently speak, and comprehend English • Proven track record as a proactive and productive team player • Valid driver's license • Able to travel domestically and internationally, including overnight stays, approximately 10–25% • Extended work hours may be necessary • Familiarity with GCLP, GLP, GMP, CLIA, and ISO regulatory guidelines (preferred) • Familiarity with Smartsheet or other project management tools (preferred) • Legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Regular full-time employment • Employee contributions and ideas valued and nurtured • Equal opportunity employer • Reasonable accommodation available during the application process

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