Job Overview
Location
Remote, Taiwan
Job Type
Full-time
Category
Product Management
Date Posted
May 4, 2026
Full Job Description
đź“‹ Description
- • The Senior/Clinical Research Associate provides overall support to study sites and clinical project teams engaged in clinical research studies, ensuring patient safety, data quality, and regulatory compliance across multiple studies.
- • Day-to-day responsibilities include overseeing study site management, conducting site visits (pre-study, initiation, routine monitoring, close-out), verifying informed consent processes, managing investigational product inventory, reviewing data for discrepancies, identifying and reporting Serious Adverse Events, and maintaining trial master files and investigator site files.
- • The role involves preparing for and attending investigator meetings, supporting site start-up activities, assisting with budget negotiations and contract execution under guidance, and communicating proactively with site personnel and project teams to resolve protocol deviations and risks.
- • The position requires travel (60-70%) and demands independent judgment, critical thinking, and the ability to work with minimal supervision in complex activities while contributing to the advancement of oncology and rare disease therapies.
- • About the team or company: Precision for Medicine is a specialized CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences, with a strong focus on oncology and rare disease to improve the speed, cost, and success of bringing life-changing therapies to patients.
- • What the person can learn or achieve: Develop expertise in global clinical trial monitoring, regulatory compliance (ICH-GCP, local regulations), investigational product management, data quality assurance, and cross-functional collaboration in a growing organization that values employee contributions and innovation in life sciences.
🎯 Requirements
- • Bachelor’s degree or international equivalent in a business, scientific, or healthcare discipline
- • Minimum of 2 years of on-site monitoring experience for CRAII; 1 year oncology and Phase I experience preferred
- • Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint)
- • Fluency in English, both verbal and written
- • Working knowledge of the drug development process
- • Willingness to travel 60-70% of the time
🏖️ Benefits
- • Opportunity to work on impactful oncology and rare disease therapies
- • Support for professional growth and idea contribution in a growing organization
- • Recognition for employee contributions and innovation
- • Flexible remote work environment with travel requirements
- • Commitment to employee appreciation and positive workplace culture
- • Equal opportunity employer with inclusive hiring practices
Skills & Technologies
About PFM Asset Management
PFM Asset Management is a distinguished investment management firm specializing in providing tailored investment solutions for institutional clients. With a strong focus on fiduciary responsibility and long-term value creation, PFM offers a comprehensive range of services including fixed income, equity, and alternative investment strategies. Their approach is grounded in rigorous research, disciplined risk management, and a deep understanding of client objectives. PFM is committed to transparency and client service, striving to be a trusted partner in helping institutions achieve their financial goals. They serve a diverse clientele, including public funds, corporate pensions, endowments, and foundations, adapting their strategies to meet unique needs.
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