Part-Time Project Manager – Veeva Vault Modules

Job not on LinkedIn

🕒 Yesterday

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of ELIQUENT Life Sciences

ELIQUENT Life Sciences

501 - 1000 employees

🧬 Biotechnology

💊 Pharmaceuticals

🤝 B2B

Biotechnology • Pharmaceuticals • B2B

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.

Apply Now

Similar Jobs

🕒 4 days ago

Check Off Your List

11 - 50

🤝 B2B

☁️ SaaS

⚡ Productivity

Remote part-time Executive Assistant supporting COYL, providing administrative assistance to clients with confidentiality and professionalism. Organizing schedules and managing communications effectively.

🕒 June 17

SharePoint Project Manager overseeing cloud-native projects with 8+ years of IT experience. Leading project management for SharePoint Online and Azure services remotely in the United States.

🕒 June 17

Associate Project Manager managing timelines and project activities for smooth delivery of key initiatives remotely. Collaborating with senior project managers on project coordination and documentation.

🕒 June 16

<Undefined>

11 - 50

🛍️ eCommerce

🏪 Marketplace

🌐 Web 3

Project Manager at Texas Health leading Salesforce CRM MVP delivery. Collaborating with teams and managing project timelines, stakeholder engagement, and resource planning.

🕒 May 19

Surgery Partners, Inc

10,000+ employees

👥 B2C

🤝 B2B

Project Manager leading complex projects and strategic initiatives from initiation to implementation in a corporate environment. Responsible for managing project timelines, budgets, and team coordination.