Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
LabConnect

Project Manager

LabConnect

. Manage and delegate responsibility for ongoing management and oversight of assigned clinical trial study projects .

Posted 11/5/2026full-timeRemote • Tennessee • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trial projects, ensuring quality deliverables, budget oversight, and effective communication with stakeholders. Proficient in project management methodologies and capable of leading multi-regional teams while maintaining compliance with laboratory practices.

Highest-signal resume keywords
Clinical Trial Project ManagementBudget ManagementStakeholder CommunicationRegulatory ComplianceTeam Leadership

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Project ManagementMetrics AnalysisReport DevelopmentProblem SolvingCalculationsQuality OversightOperational Analysis
Soft Skills
Interpersonal SkillsOrganizational SkillsCritical ThinkingStress ManagementEffective Communication
Tools & Technologies
Microsoft OfficeSharePointSalesforceMicrosoft Visio
Certifications & Qualifications
ASCP Medical Technologist CertificationRegistered Nurse Certification
Industry Keywords
Clinical TrialsLaboratory ManagementClient SpecificationsGlobal ProjectsStudy Protocols

About the role

Key responsibilities & impact
  • Manage and delegate responsibility for ongoing management and oversight of assigned clinical trial study projects
  • Direct activities to meet client specifications and ensure quality deliverables are completed on time and within budget
  • Provide ongoing oversight of clinical trial projects, including client meetings and communications, report development and review, issue resolution, and budget oversight
  • Independently lead medium- to high-complexity, multi-regional global projects involving more than two regions
  • Oversee and lead supporting co-project managers and regional LabConnect project managers as applicable
  • Participate in handover processes between Business Development, Project Set-Up, and Project Management teams
  • Participate in internal staff training and create training materials for investigator meetings as applicable
  • Serve as primary project contact for Sponsors and Contract Research Organizations
  • Serve as first point of contact for clinical-trial management issues
  • Coordinate with clinical laboratory management and directors
  • Maintain project dashboards and risk registers
  • Review enrollment logs, pending test reports, laboratory reports, issue logs, shipping manifests, and other study oversight documents
  • Review and analyze operational, quality, and performance metrics
  • Liaise with managers and supervisors across departments regarding operational changes
  • Collaborate with project managers in partner laboratories to provide a global study-management overview
  • Coordinate with internal and external teams to ensure contracted support and deliverables are met
  • Coordinate requests for shipment of stored samples according to the statement of work
  • Ensure laboratory requirements in study protocols are managed according to expectations and compliant with laboratory practices
  • Represent LabConnect at client and investigator meetings
  • Perform other related duties as assigned

Requirements

What you’ll need
  • Bachelor's degree (B.A./B.S.) from four-year college or university and two years of central laboratory project management experience
  • Associate's degree (A.A./A.S.) considered with 3+ years of central laboratory project management experience
  • Certification as an ASCP Medical Technologist and/or Registered Nurse is beneficial, but not required
  • Experience in customer service
  • Excellent organization, interpersonal, communication, and critical thinking skills
  • Ability to manage stress
  • Ability to read and interpret complex business, technical, and regulatory materials
  • Ability to write clear reports and procedures and present information effectively to stakeholders
  • Proficiency in calculations, budget management, and mathematical concepts related to clinical trial budgeting and metrics analysis
  • Ability to solve practical problems, interpret diverse instructions, and navigate situations with limited standardization
  • Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint)
  • Experience with SharePoint, Salesforce, and Microsoft Visio is a plus

Benefits

Comp & perks
  • Equal Opportunity Employer committed to diversity and inclusion
  • Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job
  • Minimal travel requirements
  • Global team environment
  • Workplace values: People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always