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Great Contract position-immediate start, CTA, Zaventem, Belgium
☞ PharmiWeb.jobs: Global Life Science Jobs
전망: 135
갱신일: 26-11-2025
범주: 법률 / 계약
산업: Staffing Recruiting
수평: Entry level
직업 종류: Contract
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작업 내용
Perfect role for available talent to start immediately and become part of a well-known company, boosting your experience and ability to develop fast professionally.This will be a perfect chance to gain some new experience, make new contacts and diversify your skills even further.Responsibilities- accountable for the timely tracking of study essential documents and ensuring completeness of the Trial Master File for assigned clinical studies according to appropriate regulations, departmental guidelines, and work instructions
- Creation/distribution of regulatory binders & the wet-ink signed documents binder
- Support ongoing use of (one) CTMS by maintaining and tracking relevant activities
- Assist study staff and investigators to quickly and effectively resolve issues relating to Study Files (Trial Master File and Investigator Site File). Respond to problems and assists in implementing corrective and preventive actions
- Bachelor’s Degree
- Previous clinical research experience is a plus
- 1+ year of Admin support experience in life science (academia, hospital, CRO, Pharma or Med Devices)
- Experience with databases and trackers
- Fluent English
- Manage multiple requests from different stakeholders and prioritise tasks in a fast passed environment
- Clinical/ medical background
- Top industry employer
- Flexibility to work 2/3 days from home
- Excellent experience on your CV that will give a boost to your career
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마감 시간: 10-01-2026
무료 후보 신청 클릭
작업 보고
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