Lifelancer
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.
Site Navigator I – II
Job not on LinkedIn
🔥 0 minutes ago
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Lifelancer
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
• Coordinate site-level activities throughout clinical study start-up and potentially closeout • Serve as the single point of contact for investigative sites from feasibility and outreach through activation and maintenance • Ensure regulatory compliance, site management, site support and training, and collaboration among sponsor, CRO, and clinical site staff • Identify and assess potential research sites • Conduct site outreach, collect confidentiality agreements, and collect feasibility surveys • Manage site-level activities, resolve issues, and support study timelines and compliance • Conduct remote pre-study visits and complete follow-up documentation • Support customization and translation of informed consent forms and patient-facing materials • Collect, track, and quality-review essential documents for site activation • Maintain site regulatory compliance, including IRB/IEC renewals, PI changes, and document expirations • Participate in study team meetings and develop action plans for site risks and issues • Support CRA teams with site initiation visit preparation and coordination of supplies, access, and documents • Submit to and liaise with IRBs/IECs, Third Bodies, and Regulatory Authorities • Conduct initial and amended contract and budget negotiations with sites • Maintain accurate filing systems and an audit-ready Trial Master File • Track start-up progress and ensure sites meet requirements and deadlines • Serve as primary contact for investigative sites and ensure timely delivery within scope and budget • Perform CRF review and data validation against source documentation • Monitor protocol deviations and Serious Adverse Event reporting • Perform country and site informed consent form review and customization • Perform other assigned duties
🎯 Requirements
• University/College degree in life science preferred, or certification in a related allied health profession from an accredited institution, or 2–3 years of clinical research experience • Relevant and equivalent experience may be considered in lieu of educational requirements • High School Diploma or equivalent plus at least 5 years of clinical research experience is an alternative qualification • Working knowledge of ICH/GCP guidelines and regulatory authority and IRB/IEC regulations • Fluent in the local official language and English, written and verbal • At least 1 year of experience in a related field, such as medical, clinical, pharmaceutical, laboratory research, data analysis, data management, or technical writing • One year of clinical research experience preferred • Basic knowledge of ICH/GCP, regulatory authorities, IRB/IEC, and applicable regulations/guidelines • Familiarity with investigator start-up documents and contract/budget negotiation processes • Understanding of research protocol requirements • Ability to communicate with site staff, CRO personnel, and regulatory authorities • Ability to manage multiple tasks and deadlines • Ability to identify and resolve start-up issues • Ability to negotiate contracts and budgets with research sites • Ability to use in-house and commercial computer software • Ability to sit for extended periods and operate a vehicle safely • Ability to perform repetitive hand movements • Ability to lift and carry 15–20 lbs • Regular and consistent attendance
🏖️ Benefits
• Remote-based work • Limited travel to training only • EEO and accommodations support • Regular and consistent attendance • Varied hours may be required
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