Clinical Scientist
Hobson Prior
- België
- Vast
- Voltijds
- Support senior clinical development staff on study protocols and amendments.
- Collaborate cross-functionally to translate strategy and approved concept into executable, efficient clinical protocols and related documents.
- Contribute to the plans to execute one or more trials in collaboration with internal/external experts.
- Author/review clinical contributions to clinical study reports (CSRs) and clinical portions of Clinical and Regulatory Documents.
- Ensure CRF design adequately supports data collection in alignment with the protocol.
- Monitor clinical data for specific trends in collaboration with cross-functional teams.
- Any other assigned duties.
- PhD in a relevant field (e.g. Neuroscience, Biomedical Sciences, Biology; chemistry: pharmacy), PharmD or MD degree from an accredited institution or Masters with relevant work experience.
- Experience in clinical research/drug development with exposure to human trial conduct with pharmaceuticals, devices, and basic clinical practice.
- Knowledge of Good Clinical Practice.
- Experience in Neurology, Psychiatry or Neuroscience is preferred.
- Experience supporting clinical studies (later stage preferred Phase II - III).
- Strong project planning/management and excellent communication skills.
- Independent decision-making and analytical skills.
- Experience working in a (virtual) matrix team environment with cross functional teams.
- Willingness to travel up to 20% of time both domestic and international.