
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.
🔥 12 hours ago
🗣️🇩🇪 German Required
🗣️🇫🇷 French Required
🗣️🇮🇹 Italian Required
🗣️🇪🇸 Spanish Required
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Ensure quality of data submitted from study sites and assure timely submission of data • Ensure appropriate reporting and follow-up for all safety events by site personnel • Ensure completeness and compile regulatory documents and ethical submission documentation, including IRB approval, informed consent, and lab certification • Provide applicable updates for site-related documentation for filing in the Trial Master File (TMF) • Perform feasibility studies and site identification activities for potential sites, as requested • Collaborate with clinical operations colleagues, customers, and sponsor contacts remotely
• Four-year college curriculum with a major concentration in life science preferred but not required • Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant • Excellent interpersonal, oral, and written communication skills • Ability to contribute to a team remotely • Strong customer focus • Ability to interact professionally with a sponsor contact • Proficiency in Microsoft Office, CTMS, and EDC Systems • Proficiency in English, Bulgarian, and one other language: German, French, Italian, or Spanish
• Supportive, team-oriented work environment • Hands-on, accessible leadership • Diverse and inclusive workplace • Equal employment opportunities • Opportunity to collaborate with colleagues across diverse backgrounds and specialties • Opportunity to contribute to scientific breakthroughs and improve patients’ lives
Apply Now🔥 19 hours ago
Remote Clinical Research Associate supporting site data, regulatory documentation, and safety reporting. Worldwide Clinical Trials advances clinical research as a global CRO.
🕒 4 days ago
Clinical Research Associate managing neurology and oncology trial sites for Worldwide Clinical Trials, a global CRO. Conducting monitoring, compliance, safety, and data-quality activities remotely in Bulgaria.
🕒 4 days ago
Clinical Trial Manager overseeing real-world evidence studies for ICON, a global healthcare intelligence and clinical research organisation. Managing clinical operations, sites, sponsors, risks, and study deliverables.
🕒 August 27
Clinical Research Associate II advancing AbbVie’s innovative medicines through compliant clinical trials. Managing investigative sites, monitoring study execution, recruitment, data quality, and patient safety.
🕒 July 9
Clinical Research Associate contributing to clinical trial monitoring and data management for ICON. Ensuring protocol compliance and high-quality data while collaborating with investigators and site staff.