Assistant CRA – FSP

🔥 2 minutes ago

🇩🇪 Germany – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 15%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Perform remote site management and monitoring activities on assigned projects • Review study data from various sources remotely • Contact study sites to collect study documentation, resolve issues and request outstanding information • Maintain collaborative communication with site staff regarding protocol conduct, enrollment, EDC completion, queries and site performance • Track and follow up on subject data in EDC and other applicable systems • Raise manual queries in EDC when applicable • Remotely review study logs • Conduct and document site management calls and contacts • Participate in investigator meetings • Investigate and follow up on centralized monitoring findings • Evaluate PI oversight, subject safety and study processes • Conduct remote risk-based investigations into site performance and support corrective/preventive actions • Provide refresher training and follow up on outstanding regulatory and administrative documents • Review clinical listings and track/trend violations, deviations, site status, enrollment, CRF status and SAE follow-up • Provide trial status tracking and progress reports to the study manager • Participate in investigator payment processes, if applicable • Liaise with internal staff to collect documents and review data and findings • Help ensure audit-ready files and CTMS/eTMF data stewardship • Contribute to company, client and regulatory audit responses

🎯 Requirements

• Bachelor’s Degree in a life science-related field • Prior clinical research experience 0-1 year, or equivalent knowledge through classwork/training • Knowledge of clinical monitoring through classwork/training • Basic medical/therapeutic area knowledge and understanding of medical terminology • Ability to attain and maintain working knowledge of ICH GCPs, applicable regulations and PPD procedural documents • Ability to successfully complete PPD’s Clinical Foundation Training Program (CFP) • Ability to successfully complete the RSM Onboarding Workshop • Fluency in German and English languages (minimum C1 Level) • Ability to evaluate medical research data • Good organizational and time management skills • Strong attention to detail • Critical thinking, root cause analysis and problem-solving skills • Good computer skills and good knowledge of MS Office • Ability to extract pertinent information from study documents, electronic study data systems, CTMS and dashboards

🏖️ Benefits

• 2 Year Fixed Term contract • Full-time (40 hours/week) • Flexible working models that support work-life balance • Clear development pathways (e.g., Senior CRA, Lead CRA, CTM) • Award-winning learning and development programme • Competitive salary • Extensive benefits package based around the health and well-being of employees • Flexible working culture • Collaborative environment • Teams of colleagues eager to share expertise and have fun together

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