Project Manager – Global Project Management, Lab Services

Precision For Medicine

. Lead new and existing CRO laboratory projects across assay development, clinical testing, biorepository/sample management and logistics, and kitting for client studies .

Posted 11/11/2026full-timeRemote • SingaporeMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management within the biotechnology and clinical trials sectors, with a strong focus on stakeholder communication, budget management, and compliance with regulatory standards. Proficient in leading cross-functional teams and driving project success through effective planning and execution.

Highest-signal resume keywords

Project Management ExperienceBudget ManagementStakeholder CommunicationRegulatory ComplianceData Analysis

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementData AnalysisBudget EvaluationRisk ManagementAssay DevelopmentClinical TestingSample ManagementLogistics CoordinationKittingDocumentation Review

Soft Skills

Interpersonal SkillsOrganizational SkillsCritical ThinkingProblem-Solving SkillsEmotional Intelligence

Tools & Technologies

MS OfficeMS 365SmartsheetProject Management Tools

Industry Keywords

BiotechnologyClinical TrialsCROGCLPGLPGMPCLIAISOLife SciencePharmaceutical

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

Employees are appreciated for their contributions
Employee input and ideas are valued and nurtured
Equal opportunity employment
Reasonable accommodation support for applicants with disabilities