Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)

Added
4 hours ago
Type
Full time
Salary
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Related skills

edc clinical research site monitoring etmf ctms

๐Ÿ“‹ Description

  • Independently conduct and document onsite and remote activities, including site monitoring and
  • Collaborate with site staff to review and ensure data consistency with source documents and study
  • Monitor, resolve and/or facilitate resolution of data queries and escalate issues as appropriate
  • Coordinate shipment of clinical supplies, including investigational product, laboratory supplies
  • Ensure site staff is trained in all aspects of the study
  • Participate in routine study progress meetings, teleconferences, and Investigator's meetings

๐ŸŽฏ Requirements

  • 4-6 years of related clinical research experience
  • (Honors) Bachelor's degree in Health Sciences, Life Sciences, Pharmacy, Nursing or equivalent
  • Fluency in written and verbal English, French and Dutch
  • Experience with Phase I-IV clinical trials
  • Thorough knowledge of ICH-GCP and local regulatory requirements
  • Proficiency in EDC systems (e.g., Medidata Rave, Oracle InForm), IRT, eTMF, CTMS

๐ŸŽ Benefits

  • Salary range: EUR 58,000 - EUR 90,500 per year
  • One-time sign-on bonus of EUR 3,000
  • Annual bonus (Short Term Incentive Program) target of 8% of annual salary
  • Monthly stipend of EUR 157.83 to offset communication costs
  • Monthly cell phone stipend of EUR 40
  • One-time expense reimbursement of up to EUR 500 for office items (scanner/printer, monitor
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