Clinical Research Associate II – Cardio

Job not on LinkedIn

🔥 2 minutes ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

💵 $79.5k - $158.5k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Manage research activities at sites participating in Worldwide’s clinical research projects • Identify potential sites for clinical research • Perform study start-up activities • Collect appropriate regulatory documents from sites • Support negotiation of contracts and budgets • Train sites to collect data properly and report potential safety-related events • Manage site activities during study maintenance • Close down research activities at sites after study conclusion • Conduct study initiation visits (SIVs) • Ensure compliance with informed consent, safety-event reporting, and regulatory requirements, primarily through remote site management

🎯 Requirements

• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to detail • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC Systems • 2+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in Cardiology or Hypertension required • Candidates must reside in the East Coast or Central United States • Willingness to travel regionally required • Must ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements

🏖️ Benefits

• Support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs • Regular touchpoints and coaching conversations with Line Manager • Clear career path and professional development leading to Clinical Trial Manager roles • Accessible Executive Leadership team • Competitive benefits package depending on location • Transparent compensation and pay equity