Preclinical Research Associate

🔥 16 hours ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $90k - $100k / year

⏰ Full Time

🟡 Mid-level

🔬 Research Analyst

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This company has sponsored H1B visas in the past.

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Eurofins

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1987

🍽️ Food & Beverage

🏥 Healthcare

📦 Logistics

💰 $30M Grant on 2021-10

Food & Beverage • Healthcare • Logistics

Eurofins is a global leader in testing and laboratory services. With approximately 62,000 employees and over 900 laboratories across 62 countries, the company provides a wide range of testing services across various industries. Eurofins offers services such as food and feed testing, consumer product testing, genomic services, clinical diagnostics, forensic services, environment testing, and pharmaceutical testing. The company is committed to scientific innovation and sustainability, and it plays a critical role in testing for health, safety, and environmental impacts worldwide.

📋 Description

• Perform quality control (QC) review of nonclinical content for DMPK and Toxicology reports • Review Module 2 and Module 4 regulatory submission documents • Provide editing, word formatting, and PDF submission-readiness support for nonclinical regulatory submission documents • Align documents with style guides and regulatory guidelines • Provide Veeva support for nonclinical regulatory document lifecycle management activities • Support literature reference-related activities, including retrieval, copyright clearance review, and upload to the electronic document management system • Independently solve problems using sound judgment, appropriate interfacing, and flexibility in a dynamic environment

🎯 Requirements

• Bachelor's degree in Life Sciences • 3 to 4+ years’ experience in relevant field • Professional certification/credentials is a plus • Experience with regulatory submissions is a plus • In-depth knowledge of Good Laboratory Practices, FDA regulations, ICH guidelines, and the drug development process • Successful track record of managing multiple projects in a fast-paced and deadline-driven environment • Impeccable attention to detail and excellent written communication skills • Proficient in Microsoft® Suite (Word, Excel, PowerPoint, Visio) • Experience with Veeva is preferred • Experience with other electronic document management and/or tracking systems is a plus

🏖️ Benefits

• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options • Life and disability insurance • 401(k) with company match • Paid vacation and holidays • Yearly goal-based bonus • Eligibility for merit-based increases • Monday-Friday 8:00am-5:00pm schedule

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