Senior Central Monitor

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 25%

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

• Perform remote site monitoring and management activities for assigned projects • Support clinical monitoring teams in implementing study strategies, initiatives, processes, and standards • Support collection of data and report generation for recruitment plans, enrollment, drug supply status, site payment status, and other clinical trial tracking • Support data risk assessments as assigned • Support monitoring teams throughout the study, including communication with clinical site institutions as appropriate • Support document collection, visit preparation, study data review, and central monitoring activities as assigned • Follow Standard Operating Procedures, regulatory requirements, ICH and GCP guidelines, and study-specific plans • Perform other duties as assigned

🎯 Requirements

• Effective communication and interpersonal skills with ability to partner with cross-functional internal and external stakeholders • Ability to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures • Ability to contribute to development of tools and processes that increase measured project efficiencies • Proficiency with clinical trial execution systems, including Electronic Document Management Systems, Electronic Data Capture Systems, and Clinical Trial Management Systems • Good understanding of general quality assurance concepts and practices • Highly organized with strong attention to detail • Bachelor’s degree preferred • Persons without a formal degree may be considered if they have comparable depth and breadth of training and experience and meet job-specific criteria • Minimum 3 years of experience in study coordination and in-house monitoring, or relevant work experience in the Biotechnology or Pharmaceutical industries or a relevant regulated environment • Working knowledge of CluePoints RBQM System desired • Long-haul COVID/Pulmonary experience desired • Compliance with FDA and/or local regulations, ICH GCPs, ProPharma Group SOPs, and project plans

🏖️ Benefits

• Remote working support • Hybrid working encouraged for new hires within a reasonably short commute of an office, as agreed with the manager • Equal Opportunity Employer workplace • Diversity, equity, and inclusion commitment • Safe and empowering workplace environment