
501 - 1000 employees
Founded 2002
🏥 Healthcare
đź’Š Pharmaceuticals
🧬 Biotechnology
đź’° $24.5M Series A - LabConnect on 2017-06
Healthcare • Pharmaceuticals • Biotechnology
LabConnect is a global central laboratory solutions partner that provides technology-driven, customized, orchestrated, and scalable laboratory and data services to support clinical trials and drug development worldwide. Its offerings include central and specialty bioanalytical testing, radiopharmaceutical support, decentralized/near-home collection, custom collection kits and high-volume kitting, companion diagnostics and assay validation, data management and harmonization, regulatory and scientific project management, and commercial/post-market support. LabConnect serves sponsors and CROs across multiple therapeutic areas (oncology, vaccines, cell and gene therapy/ATMPs and more), emphasizing program oversight and operational execution for clinical research.
đź•’ August 18
🎸 Tennessee – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
👷‍♀️ Project Manager
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501 - 1000 employees
Founded 2002
🏥 Healthcare
đź’Š Pharmaceuticals
🧬 Biotechnology
đź’° $24.5M Series A - LabConnect on 2017-06
Healthcare • Pharmaceuticals • Biotechnology
LabConnect is a global central laboratory solutions partner that provides technology-driven, customized, orchestrated, and scalable laboratory and data services to support clinical trials and drug development worldwide. Its offerings include central and specialty bioanalytical testing, radiopharmaceutical support, decentralized/near-home collection, custom collection kits and high-volume kitting, companion diagnostics and assay validation, data management and harmonization, regulatory and scientific project management, and commercial/post-market support. LabConnect serves sponsors and CROs across multiple therapeutic areas (oncology, vaccines, cell and gene therapy/ATMPs and more), emphasizing program oversight and operational execution for clinical research.
• Manage and oversee assigned clinical trial study projects • Delegate responsibility for ongoing project management and oversight • Direct activities to meet client specifications and ensure quality deliverables are on time and within budget • Provide ongoing oversight, including client meetings, communications, report development and review, issue resolution, and budget oversight • Lead medium- to high-complexity, multi-regional global projects, including oversight of supporting co-PMs and regional LabConnect PMs • Participate in handover between Business Development, Project Set-Up, and Project Management teams • Train internal staff • Serve as primary project contact with Sponsors and Contract Research Organizations • Maintain communication channels and reporting schedules • Serve as first point of contact for clinical-trial management issues • Coordinate with clinical laboratory management and directors • Maintain project dashboard and risk register • Review enrollment logs, pending test reports, laboratory reports, issue logs, shipping manifests, and other study oversight documents • Analyze operational, quality, and performance metrics • Liaise with managers and supervisors across departments • Collaborate with partner-laboratory project managers to provide a global study-management overview • Coordinate with internal departments and external project-management personnel to ensure contracted support and deliverables • Coordinate shipment requests for stored samples as directed in the SOW • Ensure laboratory requirements in study protocols are managed appropriately and comply with laboratory practices • Create training materials for investigator meetings • Represent LabConnect at client and investigator meetings • Perform other related duties as assigned
• 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 • Excellent organization, interpersonal, communication, and critical thinking skills • Adept at stress management • Ability to read and interpret complex business, technical, and regulatory materials • Ability to write clear reports and procedures and present information effectively to stakeholders • Proficient in performing calculations, managing budgets, and applying mathematical concepts to clinical trial budgeting and metrics analysis • Skilled in solving practical problems and interpreting diverse instructions in situations with limited standardization • Proficient in Microsoft Office (Outlook, Word, Excel, PowerPoint) • Minimal travel required • ASCP Medical Technologist certification and/or Registered Nurse certification beneficial but not required
• 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
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