Job Description
About you:
- Calm, thoughtful, and responsive when things don’t go as planned.
- Well-prepared, whether it be for an investigator meeting, site visit or project team update.
- Find quick and creative ways of overcoming difficulties.
How we will keep you busy and support your growth:
- Monitor and own the progress of clinical studies at investigative sites.
- Coordinate all necessary activities required to set up and monitor a study.
- Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
Qualifications:
- Life science degree and / or equivalent experience.
- 1 year or more as a CRA in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies.
- Site management or equivalent experience in clinical research.
About Precision for Medicine
Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences to improve the speed, cost and success rate of bringing life-changing therapies to patients. They have a strong focus on Oncology and Rare Disease and boast extremely high CRA retention rates compared to industry averages.