This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork - the largest global platform for the LGBTQ+ business community.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office What You'll Do Study & Site Support Complete assigned study and site management activities in accordance with the study task matrix. Complete required study-specific training and become proficient in relevant study systems. Support remote review and collection of applicable site assessments and documentation.

Verify document collection and submission status and ensure site information remains accurate and up to date. Support the collection, review, and maintenance of Essential Documents in applicable clinical systems. Coordinate requests for study system access for relevant site staff and support access maintenance throughout the study.

Follow up on required site staff training.

Study

Monitoring & Data Support Support ongoing remote review of centralized monitoring tools and study dashboards. Follow up on missing study vendor data, such as ECGs, laboratory samples, and electronic diaries, as directed. Perform reconciliation activities across assigned studies, including CRF and query status, protocol deviations, SAEs, and safety reports, as applicable.

Extract and review relevant information from study documentation, electronic study data systems, CTMS, and dashboards. Support CRAs and Clinical Leads with additional site management and remote monitoring activities as assigned.



Site Payments & Administration Support site payment processes by coordinating with investigational sites and internal functional teams.

Assist with system updates, payment reconciliations, and follow-up on site invoices throughout the study. Complete administrative activities, including timesheets and expense reports, accurately and on time. Contribute to other study-specific activities according to project and client requirements.

What We're Looking For Minimum Qualifications Bachelor's degree in a life sciences discipline or related field , Registered Nursing qualification, or equivalent relevant academic/vocational qualification. 0-2 years of relevant professional experience , making this an excellent opportunity for candidates looking to develop their career in clinical research. Equivalent combinations of education, training, and directly related experience may also be considered.

Preferred Skills &

Experience Basic understanding of medical terminology and therapeutic areas. Interest in developing a strong working knowledge of ICH-GCP , applicable regulations, and clinical research procedures. Excellent interpersonal skills and a strong customer-focused approach. Flexible and adaptable approach to changing priorities and project requirements.



Proficiency in Microsoft Office and confidence in learning new clinical trial systems and digital tools. Ability to work with study documentation, electronic clinical systems, CTMS platforms, and dashboards.

Excellent

English language skills , both written and spoken.

Working

Environment & Travel This position is primarily performed in an office or home-office environment , depending on business requirements. The Assistant CRA role does not involve regular travel . Occasional travel to clinics, hospitals, or other study locations may be required.

The position provides valuable experience and development opportunities for those interested in progressing within the CRA career path. Please note that future CRA positions typically involve significantly more travel, often approximately 60-80% , depending on the role, project, and business requirements. An excellent opportunity to start or develop your career in clinical research .

Exposure to innovative global clinical trials and international project teams. The opportunity to learn from experienced CRAs and clinical research professionals. Structured learning and opportunities to build your clinical operations expertise.

Professional development and opportunities for career progression. Competitive compensation and benefits. The opportunity to contribute to clinical research that can make a meaningful difference in patients' lives. xrdztoy If you're detail-oriented, motivated to learn, and excited about building a career in clinical research, we'd love to hear from you.

📌 Assistant Cra (Bologna)
🏢 Thermo Fisher Scientific
📍 Bologna