In-House CRA II

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $68k - $70k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🚫👨‍🎓 No degree required

👻 Ghost score 20%

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

• Serve as contact for project teams and investigative sites • Conduct and document site contacts, including contact reports for telephone sessions • Monitor site performance and implement action plans with the CRA • Support recruitment tracking and discuss study risks and opportunities with the Project Manager and CTL • Assist CRAs with site-visit preparation, report running, file quality control and action-item resolution • Oversee site maintenance activities and compliance with renewals, local regulatory and IRB/IEC requirements • Perform Case Report Form review and query generation/resolution in data management systems • Conduct assigned on-site monitoring tasks, including CRF review, SDR/SDV, Site Regulatory File review and drug accountability • Perform remote monitoring visits, including remote SDV/SDR after MEA training • Liaise with laboratories, sponsors, medical monitors, project teams and CTAs • Provide site training by phone or teleconference/web meeting • Conduct IVRS/IWRS review and reconciliation • Coordinate study visits and shipment of drug and laboratory samples • Manage sites to support protocol compliance, study visits and timelines • Distribute and track clinical trial supplies • Enter weekly study details in CTMS and assist with status reports • Assist with Ethics Committee and Regulatory Authority submissions and notifications • Facilitate translation and back translation of necessary documents • Complete project-related administrative tasks such as recruitment tracking and site document preparation • Attend and present at investigator, sponsor, kick-off and face-to-face meetings • Ensure compliance with Fortrea SOPs and local regulatory requirements • Perform other duties as assigned

🎯 Requirements

• University or college degree in biological or life science preferred, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology) • In lieu of the above, 2 or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered • Minimum of 2 years of industry experience in a related role • Basic understanding of ICH-GCP guidelines • Basic understanding of the clinical trial process • Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP • Ability to work within a project team • Good planning, organization, time management and problem-solving skills • Good oral and written communication skills • General computer literacy • Ability to work efficiently and effectively in a matrix environment • Ability to sit for extended periods and operate a vehicle safely • Ability to perform repetitive hand movements and occasional crouching, stooping, bending and twisting • Ability to use a variety of computer software • Ability to lift and carry 15–20 lbs. • Regular and consistent attendance • Varied hours may be required

🏖️ Benefits

• Remote work option • Fortrea Monitoring Excellence Academy (MEA) training program • Travel opportunities, including domestic and international travel • Equal employment opportunity and accommodations support