Project Manager – FSP Trial Lead

Job not on LinkedIn

🕒 August 26

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 43%

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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Lifelancer

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2020

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Pre Seed Round on 2022-03

Consulting • Healthcare • Logistics

Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.

📋 Description

• Serve as Project Lead and primary sponsor contact • Accountable for overall project delivery, including quality, time, and cost • Establish and communicate customer expectations to the project team • Ensure internal and external escalation pathways are followed • Lead cross-functional project teams to meet or exceed deliverables • Participate as part of the Study Management Team (SMT) • Implement and execute study plans to support successful clinical trial delivery • Work closely with global trial and functional leads • Clarify responsibilities and communication pathways for secondary project leads when required • Demonstrate financial stewardship at the trial level, including contract understanding, resource alignment to budget, out-of-scope activity management, Con Mod negotiations, and timeline execution • Establish, communicate, and manage customer expectations throughout the project • Drive project-level risk identification and issue resolution • Ensure compliance with organization policies, SOPs, ICH-GCP, regulatory requirements, and project-specific requirements • Manage vendors when required • Delegate and prioritize the workload of project team members in a frequently changing environment

🎯 Requirements

• B.A. or B. Sc. in a scientific discipline • 8+ years of comparable experience • 2+ years of project/trial management experience • Related scientific and clinical expertise • Exceptional project-management, risk-assessment, contingency-planning, and communication skills • Extensive knowledge of clinical development related to one or more trial phases (I, II, III) • Cross-functional drug development knowledge • Expertise in Good Clinical Practices (GCP), International Council for Harmonization (ICH) guidelines, and regulatory requirements for clinical development • Ability to establish and execute operational plans • Technical and systems competency, including Microsoft Outlook, Word, Excel, PowerPoint, and organization systems • Ability to delegate and effectively prioritize work in a frequently changing environment • Effective oral and written communication and presentation skills • Proactive, solutions oriented, and adaptable to changing priorities and situations • Ability to negotiate, persuade, and influence others, including cross-cultural awareness • Prior neurology therapeutic experience required • Rare-disease experience preferred • Investigator site and/or monitoring experience preferred • Functional Service Provider (FSP) experience preferred • Ability to travel domestically and internationally • Advanced degree in a related field preferred

🏖️ Benefits

• Ability to travel domestically and internationally