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eClinical Solutions

Project Management Manager

eClinical Solutions

. Oversee a team of Project Management professionals and drive operational excellence across Biometrics Services .

Posted 11/10/2026full-timeRemote • United StatesSeniorLead💰 $150,000 - $165,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates extensive experience in managing complex clinical trial projects while ensuring adherence to PMI-compliant practices and industry standards. Proven ability to lead teams, drive operational excellence, and foster strong client relationships in high-pressure environments.

Highest-signal resume keywords
Project Management Professional (PMP) Certification10+ Years of Project Management Experience5+ Years in Pharmaceutical/Biotechnology IndustryExpert Knowledge of ICH/GCP GuidelinesStrong Communication and Stakeholder Management Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Project ManagementClinical Trial ManagementData ManagementRisk ManagementOperational ExcellenceStrategic PlanningQuality AssuranceVendor ManagementAgile MethodologiesProcess Improvement
Soft Skills
LeadershipNegotiationCommunicationMentoringProblem-Solving
Tools & Technologies
Microsoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft ProjectMicrosoft VisioMicrosoft TeamsOneDriveSharePointBilling SystemsHR Systems
Certifications & Qualifications
Project Management Professional (PMP)
Industry Keywords
Biometrics ServicesClinical TrialsEDC PlatformsCRO ModelsBiotechnologyPharmaceuticalICH GuidelinesGCP Guidelines21 CFR Part 11EClinical Solutions

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Oversee a team of Project Management professionals and drive operational excellence across Biometrics Services
  • Provide leadership for high-profile and strategically important client engagements
  • Monitor, mentor, and audit direct reports for adherence to PMI-compliant practices and eClinical Solutions standards
  • Coach project managers on balancing aggressive delivery goals with realistic execution plans
  • Lead and oversee complex clinical trial projects
  • Ensure project plans account for interdependencies across EDC, IRT, CROs, sponsors, biostatistics, and data review workflows
  • Identify and manage risks related to data quality, timelines, resourcing, and external vendor dependencies
  • Drive disciplined study start-up planning and cross-functional alignment
  • Integrate lessons learned to improve delivery models and client engagements
  • Support strategic initiatives for scaling the Biometrics Services organization
  • Serve as customer success champion for assigned clinical trial clients
  • Build trusted sponsor partnerships and reinforce shared accountability for timelines and deliverables
  • Perform other duties as assigned

Requirements

What you’ll need
  • Bachelor's degree or equivalent work experience preferred
  • Project Management Professional (PMP) certification preferred
  • 10+ years of project management experience preferably in a clinical, biomedical, or software environment preferred
  • 5+ years in Pharmaceutical/Biotechnology industry or equivalent senior consulting role managing large complex clients/multiple projects preferred
  • 3+ years of people leadership preferred
  • Exceptional communication, negotiation, and stakeholder management skills
  • Strategic thinking and ability to translate vision into operational execution
  • Ability to manage ambiguity and high-pressure client environments
  • Commitment to delivery quality, client success, and organizational integrity
  • Expert knowledge of Microsoft applications including Word, Outlook, Excel, PowerPoint, Project, Visio, and Teams
  • Experience with collaborative platforms including OneDrive and SharePoint
  • Experience with operational tools including billing, HR, and payroll systems
  • Extensive experience managing complex data management/clinical trial projects and programs according to PMI and industry best practices
  • Strong working knowledge of ICH/GCP guidelines, 21 CFR Part 11, clinical trial methodologies and lifecycle, CRO and IRT vendor models, and EDC platforms such as Medidata Rave

Benefits

Comp & perks
  • Remote work
  • Work-life balance
  • Inclusive culture
  • Opportunities to learn, grow, and continuously improve
  • Company-approved AI tools to improve productivity and quality
  • Equal opportunity employment