Job Overview
Location
Remote, United States
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • The Clinical Research Associate II (CRA II) role at Precision Medicine Group is a seasoned, experienced professional responsible for monitoring and site management in clinical research studies, ensuring patient safety, data quality, and regulatory compliance across Oncology or Cardiology therapeutic areas.
- • Day-to-day responsibilities include conducting site visits (pre-study, initiation, routine monitoring, close-out), verifying informed consent processes, managing investigational product inventory and administration, reviewing site files and trial master files, resolving data discrepancies, identifying and reporting Serious Adverse Events, escalating site risks, and supporting audit readiness through accurate documentation and communication with site personnel and project teams.
- • Precision Medicine Group is a midsized, precision-focused CRO dedicated to advancing oncology and complex disease research through integrated clinical trial designs, biomarker analytics, and medical expertise, offering CRAs a supportive environment with high retention rates, meaningful influence, and strong work-life balance due to reasonable travel and direct management support.
- • In this role, the CRA II will deepen expertise in clinical trial monitoring, GCP compliance, and therapeutic area knowledge while developing leadership in site management, audit preparation, and cross-functional collaboration, with opportunities to contribute to protocol adherence, data integrity, and patient safety in high-impact oncology and cardiology studies.
🎯 Requirements
- • 4-year college degree or equivalent experience in a scientific or healthcare discipline
- • Two (2) or more years of experience as a CRA in a CRO or equivalent relevant clinical research experience
- • Excellent communication and organizational skills; ability to work as a team player with a client-focused approach
- • Proficiency with computerized information systems, electronic spreadsheets, word processing, and email
- • Ability to travel overnight, with up to 60% travel on average based on regional needs, including international travel as required
- • Fluency in English (and local language for non-English speaking countries where applicable)
🏖️ Benefits
- • Paid time off and volunteer time off
- • Robust medical offerings
- • Non-vested 401k with company match
- • Paid parental leave
- • Discretionary annual bonus, health insurance, retirement savings, life and disability benefits
- • Support for professional growth and high CRA retention rates due to positive work culture and management support
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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