• Local responsibility for the delivery of the studies at allocated sites • Monitoring the study conduct to ensure proper delivery • Preparation, initiation, monitoring, and closure of assigned sites • Trains, supports, and advises Investigators and site staff • Ensures inspection readiness of the sites • Performs monitoring visits (remote and onsite)

• Oversee Monitoring Responsibilities and Study Conduct • Ensure regulatory, ICH-GCP and protocol compliance • Collaborate with the Site Manager • Monitor site compliance and data integrity • Verify informed consent process and confidentiality protection

Role Description The position responsibilities include supporting the BRAVE (Bioaerosol Risk Assessment interVention Engineering) initiative in conducting research in the Durham/Research Triangle Park, NC area. - The position requires the candidate to travel between two daycare centers (one in Durham and one in Research Triangle Park) on Monday mornings to change filters and batteries in air samplers. - The candidate will then mail the removed filters to a research lab for testing and recharge the batteries. - Expected to take 3-4 hours/week. Qualifications - Currently pursuing a Bachelor of Science (B.S.) or higher degree in a STEM field - Availability Monday mornings at 7:30 am – 10:30 am (or Tuesday if Monday is a holiday) - Transportation between two locations - Ability to safely use a small ladder to access items above a ceiling - Precision and attention to detail Requirements - Experience in collecting and handling air samples using standard sampling techniques - Skilled in troubleshooting and maintaining air sampling pumps - Background in aerosol science, including sampling, analysis, and related laboratory methods Benefits - Pay Band: 3 - Overtime Status: Non-Exempt: Eligible for overtime - Appointment Type: Regular - Salary Information: $25 per hour - Hours per week: 10 - Review Date: 05/14/2026 - The successful candidate will be required to have a criminal conviction check. Company Description Dedicated to its motto, Ut Prosim (That I May Serve), Virginia Tech pushes the boundaries of knowledge by taking a hands-on, transdisciplinary approach to preparing scholars to be leaders and problem-solvers. - A comprehensive land-grant institution that enhances the quality of life in Virginia and throughout the world. - Virginia Tech is an inclusive community dedicated to knowledge, discovery, and creativity. - The university offers more than 280 majors to a diverse enrollment of more than 36,000 undergraduate, graduate, and professional students. - A leading global research institution, Virginia Tech conducts more than $650 million in research annually. - Virginia Tech endorses and encourages participation in professional development opportunities and university shared governance.

Role Description Are you an experienced Clinical Research Coordinator ready to step into a Clinical Research Associate (CRA) role—or a newly appointed CRA looking to strengthen your monitoring skills? We are seeking motivated and detail-oriented professionals to join our CRA team in Queensland. This opportunity is ideal for CRCs looking to transition into monitoring, as well as junior CRAs who are early in their careers and eager to build a strong foundation. Key Responsibilities - Performs and coordinates all aspects of the clinical monitoring and site management process, including but not limited to: source data review (SDR) and verification (SDV), visit reports, maintain accurate study documentation, identify & address site issues and action items. - Conducts on-site and remote site visits to assess protocol and regulatory compliance and manages required documentation. - Ensure trials are conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects' rights, well-being and data reliability. - Ensures audit readiness. - Develops collaborative relationships with investigational sites. - Collaborate with cross-functional teams, including Clinical Trial Managers, Study Start-Up and Regulatory teams. Qualifications - Minimum 5+ years’ experience as a Clinical Study/Research Coordinator working on sponsor-driven trials, or an early-career Clinical Research Associate (approximately 6–12 months’ experience). - Bachelor’s degree in life sciences, nursing, or a related field. - Solid understanding of clinical trial processes and ICH-GCP guidelines. - Strong attention to detail, time management, and organisational skills. - Critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving. - Good oral and written communication skills, with the ability to communicate effectively with medical personnel. - Ability to work in a team or independently as required. - Strong computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software. - Strong English language and grammar skills. - Ability to remain flexible and adaptable in a wide range of scenarios. - Ability and willingness to travel extensively (approximately 70–80%). - Valid Australian driver’s licence and ability to travel independently to sites. - Australian citizen or permanent resident only. Benefits - Structured CRA onboarding and training program tailored to your experience level. - Mentorship and clear progression pathway to independent CRA. - Exposure to a vast variety of clinical trials across different therapeutic areas and sponsors. - Competitive salary, car/travel allowance, and benefits. - Supportive and collaborative team culture. - Health & Wellbeing: Comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues. - Flexibility: Balance your work and personal life with flexible arrangements. - Extra Leave: Generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave. - Charitable Giving & Volunteering: Paid volunteer time to support non-profit organizations that matter to you. - Learning & Development: Access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.