Registry Manager

Job not on LinkedIn

🔥 16 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Just posted.
• Jobs at this company usually fill in 26 days.
• No salary listed.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Serve as a key team member responsible for day-to-day operations at assigned participating sites • Work on site problems of moderate scope, evaluating identifiable factors and selecting methods to obtain solutions • Interface with sites participating in the assigned registry • Communicate site concerns and issues to registry management • Implement and facilitate protocol execution and regulatory compliance during site initiation and throughout site participation • Identify and support site staff with data queries in a timely manner • Conduct SIV, Remote Site Management, and Metric Review visits • Maintain registry Master File documentation and performance • Identify and communicate poor-performing sites in a timely and appropriate manner • Provide input to registry timelines, procedures, forms, support materials, manuals, and tracking systems as requested by the manager • Network with senior internal and external personnel in the area of expertise

🎯 Requirements

• Bachelor’s degree, preferably in life sciences, public health, health services research or related area, and/or equivalent experience • 4+ years’ experience in a clinical research setting • Knowledge and utilization of MS Office, Salesforce, REDCap Cloud, and Zelta EDC platforms • GCP and HSP training certificate required per policies and procedures • Advanced degree, research, and regulatory certifications such as RAPS or ACRP certificates preferred • Ability to write clear and complete assignments with attention to detail and a high degree of accuracy • Strong interpersonal skills • Ability to manage multiple study timelines, sites, and subscribers’ commitments • Experience analyzing and interpreting written material and quantitative data to draw conclusions and make recommendations preferred • Proficiency in accessing information stored in large data systems

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Accessibility services and accommodations for job seekers with disabilities

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