Senior Associate, Pharmacovigilance – Japan

Job not on LinkedIn

🔥 14 hours ago

🇯🇵 Japan – Remote

⏰ Full Time

🟠 Senior

✨ Associate

👻 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

• Author Safety Management Plans for assigned studies • Attend internal and client meetings as appropriate • Attend and present at Investigator Meetings • Review incoming SAE data for completeness and accuracy • Perform data entry in the Safety Database and/or track incoming safety information • Generate queries for missing or unclear information and follow up with sites for resolution • Perform quality control of SAEs processed by other Pharmacovigilance Associates • Generate regulatory reports and perform safety submissions as needed • Prepare and submit periodic safety reports as needed • Maintain knowledge of safety-related regulations and guidelines • Maintain basic understanding of project budgets and scope of work, ensuring compliance and escalating potential scope changes • Assist with bid defenses or other presentations • Mentor or train new Pharmacovigilance staff • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree in a science-related field or nursing, or equivalent • Equivalent combination of relevant education and experience • Minimum of 5 years of pharmacovigilance experience in pre-approval clinical trials • Excellent understanding of medical and scientific terminology • Understanding of clinical assessment principles for adverse drug events • Understanding of international regulations and reporting requirements • Understanding of computer technology and relational database systems, including data extraction • Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word) • Excellent written and verbal communication skills • Ability to work independently and prioritize work effectively • Ability to work successfully in a matrix team environment • Ability and willingness for potential limited domestic and international travel as needed • Fluent in written and verbal English

🏖️ Benefits

• Diverse and inclusive work environment • Supportive and cohesive teams • Accessible, hands-on leaders • Potential limited domestic and international travel as needed