Clinical Research Associate I
Austin, TXResearchSeen 5 days agoSeen in employer's feed 5 days ago
Most applications go out cold — see where you stand first. No sign-up to start.
Watch jobs like this. New roles like this one near Austin, TX, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Job overview
The Clinical Research Associate I supports clinical studies across multiple sites by coordinating site performance, participant recruitment and retention, data collection, and regulatory compliance. The role maintains study records and documentation, assists with reports and publications, and contributes to protocol development, staff training, and audits. It also requires organized, detail-oriented work, clear communication, analysis, problem-solving, and effective task prioritization.
Skills & qualifications
Skills
Full job description
:Site Management Ensures compliance with study protocols and regulatory requirements. Manages site performance and resolves issues.Data Collection and Management Conducts participant interviews. Ensures accurate and timely data entry into electronic data capture systems. Reviews and resolves data queries.Regulatory Compliance Ensures adherence to Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines. Facilitate institutional review board (IRB) applications, submissions, and updates across multiple sites. Prepares and maintains regulatory documents. Coordinates with ethics committees to safeguard participant rights.Participant Recruitment and Retention Coordinates with clinical partners to identify eligible study participants. Assists in screening, enrolling, and consenting of study participants. Maintains communication with participants to ensure retention. Addresses participant concerns and queries.Reporting and Documentation Prepares study reports and documentation. Maintains accurate records of study activities. Assists in the preparation of manuscripts and publications.MARGINAL OR PERIODIC FUNCTIONS: Conducts literature reviews to support study design and protocol development. Assists in the training of new site staff and research team members. Participates in internal and external audits. Supports the development of study protocols and case report forms. Attends conferences and workshops to stay updated on industry trends. Adheres to internal controls and reporting structure. Performs related duties as required.KNOWLEDGE/SKILLS/ABILITIES Double-checks work for errors, maintains organized records, and follows detailed procedures. Writes clear and concise reports, actively listens to others, and presents information effectively. Analyzes information, develops solutions, and implements corrective actions. Shares information, supports team decisions, and contributes to team success. Prioritizes tasks, sets realistic deadlines, and uses time efficiently.
Similar jobs, posted recently
Open roles like this one, listed in the last 30 days.
- Research Associate IUNIVERSITY OF TEXAS AT AUSTIN · Austin, TX
Clinical Research Associate (CRA) - Oncology - US Any RegionParexel · Austin, TX
Research Engineering Scientist Associate I - Austin, TXUNIVERSITY OF TEXAS AT ARLINGTON · Austin, TX · $45–50K/yr- Clinical Research CoordinatorUNIVERSITY OF TEXAS AT AUSTIN · Austin, TX
- Social Science/Humanities Research Associate IUNIVERSITY OF TEXAS AT AUSTIN · Austin, TX
You've read the whole posting — now see how you match it.