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About You:
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You have an impeccable eye for detail.
How we will keep you busy and support your growth:
- You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol.
- You will coordinate all necessary activities required to set up and monitor a study.
- You will identify potential study risks and propose solutions on how to mitigate them.
Qualifications:
- Life science degree and / or equivalent experience.
- At least 6 months experience as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
- Excellent communication and organizational skills are essential.
Precision for Medicine
Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences to improve therapies for patients, with a focus on Oncology and Rare Disease. They cultivate a culture, and have high CRA retention rates.