Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
Assistant CRA, m/f/d
Job not on LinkedIn
🕒 May 31
🗣️🇩🇪 German Required
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
📋 Description
• perform remote site management and monitoring activities on assigned project(s) • contact study sites to collect study documentation, resolve issues and request outstanding information • develop and maintain a close and collaborative communication with the site staff • actively discuss protocol conduction, enrollment rates and strategies, open issues, EDC completion and queries • complete/track/follow up ETRTR for subject data present in the EDC • remotely review study logs as deemed necessary • conduct and document site management calls/contacts • investigate and follow-up on centralized monitoring findings • evaluate PI oversight, subject safety and study processes • conduct remote investigations into site performance using a risk based monitoring approach • provide refresher training, follow up on outstanding administrative needs • review ad-hoc clinical listings review, track and trends violations and deviations
🎯 Requirements
• Bachelor’s Degree in a life science-related field • Prior clinical research experience 0-1 year • knowledge of clinical monitoring through classwork/training • basic medical/therapeutic area knowledge • understanding of medical terminology • ability to attain and maintain a working knowledge of ICH GCPs • 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 • effective oral and written communication skills • good organizational and time management skills • strong attention to detail • ability to work in a team or independently • well-developed critical thinking skills • good computer skills with knowledge of MS Office.
🏖️ Benefits
• continued career advancement opportunities • award winning training • benefits focused on the health and wellbeing of our employees • flexible working culture
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