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) is a seasoned professional responsible for monitoring and site management in clinical research studies, ensuring patient safety, data quality, and regulatory compliance across all phases of trial execution.
- • Day-to-day responsibilities include conducting site visits (pre-study, initiation, routine, and close-out), verifying informed consent processes, reviewing investigator site files and trial master files, managing investigational product inventory and reconciliation, identifying and reporting serious adverse events, resolving data discrepancies via EDC and patient profile reviews, and preparing accurate monitoring reports.
- • The role involves supporting site start-up activities such as feasibility assessments, investigator recruitment, EC/IRB submissions, contract negotiations, and document preparation, as well as assisting with budget finalization under guidance from Site Contract Management.
- • The CRA II works independently as part of a study team, communicates proactively with site personnel and internal project teams, develops strong relationships with investigators, and serves as an ambassador for Precision Medicine Group’s commitment to quality and professionalism.
- • Precision Medicine Group is a global leader in precision medicine, providing integrated clinical research services to biopharma clients, with a focus on delivering high-quality, compliant, and efficient clinical trial execution across diverse therapeutic areas.
- • In this role, the individual will deepen expertise in clinical trial monitoring, GCP compliance, risk-based monitoring, and cross-functional collaboration, while gaining experience in complex therapeutic areas such as oncology, autoimmune diseases, and rare conditions, positioning them for advancement into senior CRA or clinical trial management roles.
🎯 Requirements
- • Minimum of two (2) years of experience as a Clinical Research Associate (CRA) in a CRO, pharmaceutical, or biotech environment
- • Bachelor’s degree in a life science, pharmacy, or related health discipline (or equivalent experience)
- • Proven experience monitoring oncology trials
- • Strong communication and organizational skills, with ability to work independently and as part of a team
- • Willingness and ability to travel up to 60% of the time, including overnight and international travel as required
- • Proficiency in computerized information systems, including electronic spreadsheets, word processing, email, and EDC platforms
🏖️ Benefits
- • Eligibility for a discretionary annual bonus
- • Comprehensive health insurance coverage
- • Retirement savings benefits (e.g., 401(k) with potential company match)
- • Life insurance and disability benefits
- • Paid time off for vacation, sick leave, and parental leave
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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