About Pharm-Olam, LLC:
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.
Under departmental supervision, researches, creates, edits, and coordinates the production of clinical documents such as study protocols and consent forms, clinical study reports and Investigators brochures. May provide writing support for more complex clinical documentation such as IMPDs, DSUR, etc. Works within a project team with project managers, data managers, statisticians, regulatory officers, medical officers to ensure the timely and efficient delivery of study documents. For stand-alone projects, may serve as primary technical contact with client under appropriate department supervision.
Please apply online at www.pharm-olam.com/careers
Pharm-Olam, LLC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.