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Project Manager
Flagship Biosciences, Inc.. Plan, initiate, oversee, and close clinical and nonclinical research projects according to Statements of Work and contracted budgets .
Posted 10/26/2026full-timeRemote • California • United StatesMid-LevelSenior💰 $60,000 - $110,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in project management within clinical and nonclinical research, with a strong focus on regulatory compliance, client communication, and cross-functional team coordination. Proficient in managing project timelines, budgets, and documentation while ensuring adherence to CAP, CLIA, and GLP standards.
Highest-signal resume keywords
Project ManagementClient CommunicationRegulatory ComplianceCross-Functional Team CoordinationPMP Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project CoordinationBudget TrackingData PresentationReport WritingTimeline ManagementSample TrackingProcess ImprovementSOP CreationAudit AssistanceClient Feedback Collection
Soft Skills
Attention to DetailOrganizational SkillsVerbal CommunicationWritten CommunicationPrioritization
Tools & Technologies
Microsoft OfficeProject Management SoftwareHistologyImmunohistochemistry (IHC)Digital Pathology/Image Analysis
Certifications & Qualifications
PMP Certification
Industry Keywords
Life ScienceCROCAPCLIAGLPPharmacologyMolecular BiologyBiochemistryDiagnostics ServicesLaboratory Regulations
Tech Stack
Tools & technologiesPMP
About the role
Key responsibilities & impact- Plan, initiate, oversee, and close clinical and nonclinical research projects according to Statements of Work and contracted budgets
- Define project scope and objectives with stakeholders and obtain required study information from clients
- Maintain projects in project management software, including timelines, milestones, and deliverables
- Monitor progress, address risks or delays, and escalate issues when needed
- Coordinate cross-functional teams and resource availability across histology, image analysis, science, pathology, quality assurance, and business development
- Coordinate study planning, setup activities, and third-party/vendor involvement
- Develop project-specific tools for tracking work and samples
- Lead project retrospectives and implement process improvements
- Serve as primary client contact and advocate throughout the project lifecycle
- Lead client kickoff, data presentation, milestone, and close-out meetings
- Document client calls and status meetings; provide updates, timelines, and deliverable tracking
- Coordinate client requests and shipping/receiving logistics
- Investigate and resolve client complaints and collect client feedback
- Coordinate sample receipt and check-in, verify shipments, and reconcile discrepancies
- Schedule studies and establish realistic turnaround times and deadlines
- Support report and protocol writing/review and data transfers
- Manage project archives, logs, charts, files, and return of materials
- Track project budgets, invoicing, project progress, and revenue forecasts
- Collaborate with Business Development to onboard and integrate new clients
- Follow SOPs, company policies, and CAP, CLIA, and GLP regulatory requirements
- Maintain study documentation, including binders for CLIA-designated studies
- Assist with audits, non-conformances, CAPAs, and SOP creation/review/update
- Complete required training and participate in the Safety Committee
- Improve workflow, lab capacity, communication, and customer satisfaction
- Perform other duties as assigned
Requirements
What you’ll need- BA/BS in a life science (e.g., Molecular Biology, Biochemistry, Pharmacology) or science related field; AA/AS considered with additional experience
- 3–5 years relevant project coordination or project management experience in a Life Science or CRO setting
- Proficient in Microsoft Office applications and project management software
- Extremely organized, with keen attention to detail, especially in written work
- Excellent verbal and written communication skills; fluent in English
- Ability to effectively prioritize and manage multiple projects simultaneously
- Flexibility to work across departments and build thorough knowledge of company processes
- PMP Certification preferred
- Experience in a CAP/CLIA- and/or GLP-regulated laboratory, CRO, or diagnostics services environment preferred
- Working knowledge of histology, immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), digital pathology/image analysis, or similar technologies preferred
Benefits
Comp & perks- Travel to client sites, partners, and scientific meetings as needed (up to 10%)
- Workshops/webinars and continuing education opportunities