CRA
Pharm-Olam International is seeking experienced Clinical Research Associates to monitor trials in Romania. This is a full time position based in our Bucharest office.
Key Responsibilities:
- Manage activities associated with studies
- Create and review informed consent, study reports and monitoring tools
- Organize and conduct investigator meetings
- Research and resolve data queries
- Interact with senior staff regarding objectives and status of clinical projects
- Prepare reports and make presentations
- Ensure regulatory compliance with FDA, ICH/GCP guidelines, and company SOP’s
Requirements:
Preferred candidates will have prior clinical trial montoring experience or be a Medical doctor who is a specialist. Applicants should have good communication skills and an eye for detail.
For confidential consideration, please send CV to hr-romania@pharm-olam.com. NO PHONE CALLS PLEASE.
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