Pharm-Olam, LLC is a mid-size Contract Research Organization (CRO) that has a massive global reach. We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam has one of the largest global footprints of any CRO today and we are committed to not only maintain our standard, but to continue to strengthen our presence even further. We offer a unique working environment with a global team culture, competitive salary and benefits package.
To ensure that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP) and International Conference on Harmonization (ICH). May be responsible for assisting the RA Department in the preparation, compilation, submission and maintenance of regulatory documentation required by international regulatory agencies for clinical trials and marketing applications.
This is a full-time opportunity for an experienced Senior Clinical Research Associate residing in the USA. Ideal candidates should have a variety of trial monitoring (field & remote) and full site management experience in areas such as Oncology, Infectious Diseases / Vaccines, Rare / Orphan Diseases, Immunology, General Medicine, etc. This position requires flexibility with travel, on average, 70-80% throughout the US. #LI-Remote
Please apply online at www.pharm-olam.com/careers
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