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About You:
- Calm, thoughtful, and responsive when things don’t go as planned.
- Well-prepared for investigator meetings, site visits or project team updates.
- Able to find quick and creative ways of overcoming difficulties.
How we will keep you busy and support your growth:
- Responsible for monitoring and owning the progress of clinical studies at investigative sites.
- Ensuring clinical studies are conducted, recorded, and reported per protocol.
Qualifications:
- Life science degree and / or equivalent experience.
- 2 years or more as a CRA in either a CRO or pharmaceutical/biotech industry.
- Site management or equivalent experience in clinical research.
Precision for Medicine
Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. They have a strong focus on Oncology and Rare Disease and passionate about cultivating their culture with high CRA retention rates.