ph3Work Schedule /h3pStandard (Mon-Fri) /ph3Environmental Conditions /h3pOffice /ph3Job Description /h3h3Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation /h3h3What You'll Do /h3h3Study Site Support /h3ulliComplete assigned study and site management activities in accordance with the study task matrix.
/liliComplete required study-specific training and become proficient in relevant study systems.
/liliProvide in-house support for pre-study assessments and related activities.
/liliSupport the customization and maintenance of site-specific documentation, including informed consent forms (ICFs), as required.
/liliSupport remote review and collection of applicable site assessments and documentation.
/liliVerify document collection and submission status and ensure site information remains accurate and up to date.
/liliSupport the collection, review, and maintenance of Essential Documents in applicable clinical systems.
/liliFollow up on missing, incomplete, or expired documentation and support resolution of outstanding document findings.
/li /ulh3Site Coordination /h3ulliSupport investigational sites throughout study start-up, activation, ongoing management, recruitment, and close-out activities, as assigned.
/liliAssist site staff with vendor qualification processes where applicable.
/liliCoordinate requests for study system access for relevant site staff and support access maintenance throughout the study.
/liliFollow up on required site staff training.
/liliCoordinate and support logistics for investigator meetings and other study activities.
/liliSupport study and site supply management throughout the study lifecycle.
/liliMaintain study and vendor trackers as assigned.
/li /ulh3Study Monitoring Data Support /h3ulliSupport ongoing remote review of centralized monitoring tools and study dashboards.
/liliFollow up on missing study vendor data, such as ECGs, laboratory samples, and electronic diaries, as directed.
/liliPerform reconciliation activities across assigned studies, including CRF and query status, protocol deviations, SAEs, and safety reports, as applicable.
/liliExtract and review relevant information from study documentation, electronic study data systems, CTMS, and dashboards.




/liliSupport CRAs and Clinical Leads with additional site management and remote monitoring activities as assigned.
/li /ulh3Site Payments Administration /h3ulliSupport site payment processes by coordinating with investigational sites and internal functional teams.
/liliAssist with system updates, payment reconciliations, and follow-up on site invoices throughout the study.
/liliComplete administrative activities, including timesheets and expense reports, accurately and on time.
/liliContribute to other study-specific activities according to project and client requirements.
/li /ulh3What We're Looking For /h3h3Minimum Qualifications /h3ulliBachelor's degree in a blife sciences discipline or related field /b , Registered Nursing qualification, or equivalent relevant academic/vocational qualification.
/lilib0–2 years of relevant professional experience /b , making this an excellent opportunity for candidates looking to develop their career in clinical research.
/liliEquivalent combinations of education, training, and directly related experience may also be considered.
/li /ulh3Preferred Skills Experience /h3ulliBasic understanding of medical terminology and therapeutic areas.
/liliInterest in developing a strong working knowledge of bICH-GCP /b , applicable regulations, and clinical research procedures.
/liliExcellent written and verbal communication skills.
/liliExcellent interpersonal skills and a strong customer-focused approach.
/liliStrong organizational and time-management skills with excellent attention to detail.
/liliAbility to manage multiple tasks efficiently and effectively.
/liliStrong critical thinking and problem-solving capabilities.
/liliFlexible and adaptable approach to changing priorities and project requirements.
/liliAbility to work effectively both independently and as part of a cross-functional team.




/liliProficiency in Microsoft Office and confidence in learning new clinical trial systems and digital tools.
/liliAbility to work with study documentation, electronic clinical systems, CTMS platforms, and dashboards.
/lilibExcellent English language skills /b , both written and spoken.
/li /ulh3Working Environment Travel /h3pThis position is primarily performed in an boffice or home-office environment /b , depending on business requirements.
/pulliThe Assistant CRA role bdoes not involve regular travel /b .
/liliOccasional travel to clinics, hospitals, or other study locations may be required.
/liliThe position provides valuable experience and development opportunities for those interested in progressing within the CRA career path.
/liliPlease note that future CRA positions typically involve significantly more travel, often approximately b*****% /b , depending on the role, project, and business requirements.
/li /ulh3Why Join Thermo Fisher Scientific?
/h3pWhen you join Thermo Fisher Scientific, you become part of a global team committed to accelerating scientific discovery and improving patient outcomes.
/ppWe offer: /pulliAn excellent opportunity to bstart or develop your career in clinical research /b .
/liliExposure to innovative global clinical trials and international project teams.
/liliThe opportunity to learn from experienced CRAs and clinical research professionals.
/liliStructured learning and opportunities to build your clinical operations expertise.
/liliA collaborative and inclusive working environment.
/liliProfessional development and opportunities for career progression.
/liliCompetitive compensation and benefits.
/liliThe opportunity to contribute to clinical research that can make a meaningful difference in patients' lives.
/li /ulpIf you're detail-oriented, motivated to learn, and excited about building a career in clinical research, we'd love to hear from you.
/ppThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
/p /p #J-*****-Ljbffr

📌 Assistant Cra (Milano)
🏢 Thermofisher Scientific
📍 Milano