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Responsibilities:
- Responsible for the oversight and management of operational activities in given regional area.
- Develop and oversee procedures for dealing with troubleshooting and problem solving.
- Support the evaluation of suitability of site personnel and facility for initial and ongoing conduct of clinical trial
Qualifications and Skills:
- Minimum 7-10 years clinical research experience as a CRA or equivalent.
- Recent experience in leading the conduct of global phase 3 studies from start to completion required.
- Excellent understanding and demonstrated application of FDA guidelines, Good Clinical Practices (GCP), ICH and applicable Standard Operating Procedures.
Location/Travel:
- This is a full-time, remote position in the US.
- Expected domestic/regional travel up to 50% with some international travel.
- Flexible schedule with interactions across North America, Europe and Israel time zones.
Prilenia
Prilenia is a private biopharmaceutical company focused on developing transformative medicines for neurodegenerative diseases. With a highly committed and talented global team, they are developing pridopidine, an investigational neuroprotective therapy for ALS and Huntington’s disease.