Senior Scientific Project Manager

Job not on LinkedIn

🔥 35 minutes ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

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Dayforce

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

👥 HR Tech

☁️ SaaS

🏢 Enterprise

💰 $1G Post-IPO Debt - Dayforce on 2024-03

HR Tech • SaaS • Enterprise

Dayforce is a cloud-based human capital management (HCM) platform developed by Ceridian. It provides an integrated SaaS application for payroll, HR, benefits, workforce management (time & attendance and scheduling), and talent management, aimed at employers and HR teams. Dayforce is marketed as a B2B solution for mid-market and enterprise organizations seeking unified HR and payroll functionality.

📋 Description

• Lead the contracting with third-party lab service providers for assay development and validation • Collaborate with business operations, procurement, and clinical teams to ensure appropriate SOWs and contracts • Manage critical reagent supply and sample analysis • Work closely with bioanalytical strategy leads, clinical trial teams, and lab service providers to finalize study documents and meet timelines • Support the development of novel Bioanalytical processes • Provide input into clinical trial documents (e.g., eCRFs, ICFs, SOWs) • Drive the delivery of data transfer specifications and ensure data accuracy • Track and reconcile sample testing, resolving any issues that arise • Contribute to cleaning and finalizing data

🎯 Requirements

• Bachelor’s, or Master’s level equivalent degree in Life Sciences or related field, required • 2 - 3 years' experience in the drug development and/or clinical trial processes for Scientific Project Manager, required • 5 - 6 years’ experience in the drug development and/or clinical trial processes for Senior Scientific Project Manager, required • Equivalent amount of experience managing projects, including timelines, budgeting and forecasting • Experience with method development, validation and troubleshooting • Extensive knowledge and experience in bioanalysis within regulatory environments (GLP/ GCP) to include experience with PK/ADA and/or biomarker analysis • Experience working in Oncology is preferred • PMP certified and formal change management training strongly preferred • Highly proficient in MS Office Suite, including MS Project, Word, Excel and PowerPoint, Smartsheet and SharePoint • Strong planning, attention to detail, communication, and organizational skills • Excellent verbal and written communication skills

🏖️ Benefits

• Fully remote position with potential for <5% travel