Part-Time Project Manager – Veeva Vault Modules

Job not on LinkedIn

🕒 June 23

🏄 California – Remote

🏄 California – Remote

💵 $75 - $100 / hour

⏱ Part Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 28%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ELIQUENT Life Sciences

WebsiteLinkedInAll Job Openings

501 - 1000 employees

💼 Consulting

🏥 Healthcare

🧬 Biotechnology

Consulting • Healthcare • Biotechnology

ELIQUENT Life Sciences is a regulatory consulting firm that provides integrated regulatory, quality, and safety solutions to life sciences companies. They support pharmaceutical, biotechnology, medical device, and combination product sponsors across the product lifecycle — from early development and CMC strategy through regulatory submissions, pharmacovigilance, quality/compliance, remediation, and post‑approval support. ELIQUENT combines former regulators, industry leaders, and technical specialists to deliver hands‑on execution and strategic guidance for global market authorization and lifecycle management.

📋 Description

• Lead and oversee complex projects within the professional, scientific, and technical services sector, ensuring successful delivery on time, within scope, and budget. • Requires strategic planning, resource coordination, and risk management to align project outcomes with organizational goals and client expectations. • Act as a liaison between stakeholders, facilitating clear communication and collaboration across multidisciplinary teams. • Analyze project performance data to identify areas for improvement and implement best practices to enhance efficiency and quality. • Drive project success by applying expert knowledge and leadership to deliver measurable business value.

🎯 Requirements

• Minimum 5+ years of project management or project coordination experience, including at least 2–4 years supporting regulated life sciences, pharmaceutical, biotechnology, GxP, quality systems, validation, or regulated documentation projects. • Project coordination or project management experience in a regulated life sciences, pharmaceutical, biotechnology, or GxP environment. • Experience tracking documentation deliverables, action items, milestones, risks, open items, and follow-ups across multiple workstreams. • Ability to coordinate cross-functional stakeholders, follow up with document owners, and maintain visibility into deliverable status. • Experience working with external vendors, implementation partners, and internal client stakeholders. • Proficiency using Microsoft Teams, Zoom, and project tracking tools to support remote collaboration. • Strong communication, organization, stakeholder management, and follow-through skills. • Availability to support a part-time remote engagement during 8:00 AM–5:00 PM PDT business hours.