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Baylor Genetics

Clinical Development Project Manager

Baylor Genetics

. Lead execution of Clinical Development projects, ensuring milestones are achieved on time, within scope, and in alignment with clinical and organizational priorities .

Posted 11/6/2026full-timeRemote • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing complex clinical development projects, ensuring compliance with regulatory standards while effectively leading cross-functional teams. Proficient in project planning, risk management, and data analysis to drive successful project outcomes.

Highest-signal resume keywords
Clinical Development Project ManagementCross-Functional Team LeadershipRisk Management and MitigationData Pipeline and Analytical Workflow ManagementProject Management Certification (PMP or Equivalent)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Project PlanningRisk Register ManagementData AnalysisGenomic AnalysisValidation ComplianceTechnical Dependency ManagementLaboratory Informatics PlatformsTimeline Adherence MonitoringProcess RigorRegulatory Compliance
Soft Skills
Excellent CommunicationOrganizational SkillsInterpersonal SkillsNegotiation SkillsProblem-Solving Skills
Certifications & Qualifications
Project Management Certification (PMP or Equivalent)
Industry Keywords
Life SciencesGeneticsMolecular BiologyClinical ResearchHealthcare AdministrationBiotechnologyDiagnosticsClinical Lab OperationsData GovernanceOperational Excellence

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Lead execution of Clinical Development projects, ensuring milestones are achieved on time, within scope, and in alignment with clinical and organizational priorities
  • Develop and manage detailed project plans, dependency maps, and risk registers
  • Proactively mitigate delivery, data, and validation risks across dry lab workflows
  • Coordinate cross-functional teams across bioinformatics, software engineering, clinical operations, and product
  • Drive execution, resolve blockers, and ensure accountability for deliverables
  • Translate complex analytical and computational requirements into clear, executable project deliverables
  • Support scalable and compliant genomic analysis and reporting
  • Monitor and analyze project performance metrics, including timeline adherence, risk trends, and validation readiness
  • Report project status, risks, and outcomes to program leadership through clear, data-driven updates and summaries
  • Support documentation, audits, and validation activities to ensure regulatory, quality, and data-governance compliance
  • Perform other duties as assigned to support team and organizational objectives
  • Comply with company policies, procedures, and applicable regulatory requirements

Requirements

What you’ll need
  • Bachelor’s degree in Life Sciences, Genetics, Molecular Biology, Public Health, Healthcare Administration, Clinical Research, or related field
  • Minimum 4 years of relevant experience in clinical lab operation, development and research, diagnostics, biotechnology, healthcare, or related fields
  • At least 2 years managing cross-functional projects with accountability for timelines and deliverables
  • Demonstrated ability to manage multiple technically complex projects simultaneously
  • Extensive experience managing cross-functional teams, including bioinformatics scientists, software engineers, analysts, and clinical stakeholders
  • Proven experience working with data pipelines, analytical workflows, or laboratory informatics platforms
  • Strong understanding of technical dependencies, system integrations, and validation considerations in regulated environments
  • Excellent communication, organizational, and leadership skills
  • Effective interpersonal, negotiation, and technical meeting facilitation skills
  • Demonstrated ability to lead teams through ambiguity, evolving technical requirements, and data-driven decision-making
  • Ability to collaborate effectively with stakeholders at all levels, including highly technical and non-technical audiences
  • Strong analytical and problem-solving skills, with the ability to identify and mitigate technical and delivery risks
  • Strong attention to detail, data accuracy, and process rigor
  • Passion for continuous improvement and operational excellence
  • Equivalent combination of education and experience may be considered
  • Master’s degree in life science, or a related field (preferred)
  • Project management certifications (PMP or equivalent) (preferred)

Benefits

Comp & perks
  • May require occasional travel to conferences, partner sites, healthcare institutions, or company meetings