Project Manager

Pharmavise Corporation

Project Manager for life sciences consulting supporting GxP and FDA-regulated projects remotely. Leading cross-functional teams and ensuring compliance across pharmaceutical, biotechnology, and medical device organizations.

Posted 5/19/2026contractRemote • 🇺🇸 United StatesMid-LevelSeniorWebsite

Tech Stack

Tools & technologies

Google Cloud PlatformPMP

About the role

Key responsibilities & impact

Lead and manage cross-functional projects within pharmaceutical, biotechnology, and/or medical device environments
Develop and maintain project plans, timelines, budgets, risk registers, and status reports
Coordinate project activities across Quality, Regulatory, Engineering, Validation, Manufacturing, Clinical, and Supply Chain teams
Facilitate stakeholder meetings and communicate project updates to client leadership and internal teams
Identify project risks, issues, and mitigation strategies to ensure successful project execution
Support project governance, resource planning, prioritization, and execution activities
Ensure projects align with applicable GxP, FDA, ISO, and industry compliance requirements
Drive accountability, action item tracking, and project deliverables across multiple stakeholders
Support continuous improvement and operational excellence initiatives
Maintain strong client relationships and represent Pharmavise professionally in client-facing environments.

Requirements

What you’ll need

Bachelor’s degree in Engineering, Life Sciences, Business, Healthcare, or related field
5+ years of Project Management experience within the life sciences industry
Experience supporting pharmaceutical, biotechnology, and/or medical device organizations
Strong understanding of GxP-regulated environments
Demonstrated experience managing cross-functional teams, timelines, budgets, and project deliverables
Excellent communication, stakeholder management, and organizational skills
Ability to work independently in fast-paced client environments
Proficiency with project management and collaboration tools such as Microsoft Project, Smartsheet, Jira, SharePoint, or similar platforms
Preferred PMP certification or equivalent project management certification
Experience within consulting or professional services environments
Experience supporting Fortune 500 life sciences companies
Knowledge of FDA, ISO 13485, 21 CFR Part 11, ICH, GMP, GLP, or GCP requirements
Experience leading global or multi-site projects.

Benefits

Comp & perks

Remote work options

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 & Tools

Project ManagementRisk ManagementBudget ManagementTimeline ManagementCross-functional Team ManagementGxP ComplianceFDA RegulationsISO 1348521 CFR Part 11GMP

Soft Skills

CommunicationStakeholder ManagementOrganizational SkillsClient Relationship ManagementLeadershipAccountabilityAction Item TrackingIndependent WorkContinuous ImprovementOperational Excellence

Certifications

PMP CertificationProject Management Certification