
51 - 200 employees
Founded 2020
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Pre Seed Round on 2022-03
Consulting âą Healthcare âą 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.
đ„ 5 minutes ago
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51 - 200 employees
Founded 2020
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Pre Seed Round on 2022-03
Consulting âą Healthcare âą 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.
âą Conduct site qualification, initiation, interim monitoring, site management, and study close-out visits âą Mentor and guide less experienced CRAs and site staff âą Document site visit findings via written reports âą Assess, monitor, and train study site staff on protocol adherence âą Review study subject safety information and informed consent âą Conduct source document verification for compliance, patient safety, and data veracity âą Review CRFs using paper or electronic data capture systems âą Assist sites with data query resolution âą Provide updates for site-related documentation for filing in the Trial Master File âą Ensure site compliance with investigational product receipt, accountability, and return or destruction âą Conduct accompanied site visits for assessment or training of other CRAs
âą Excellent interpersonal, oral, and written communication skills in English âą Superior organizational skills with attention to detail âą Ability to work with little or no supervision âą Proficiency in Microsoft Office, CTMS, and EDC systems âą 5+ years of experience as a Clinical Research Associate âą 4-year university degree or RN/BSN in Nursing âą Willingness to travel âą Ability to conduct clinical trial site qualification, initiation, interim monitoring, site management, and study close-out visits
âą Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law âą Supportive and cohesive teams âą Diverse and inclusive work environment âą Remote work arrangement
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