Clinical Technical Editor / Scientific Document Reviewer - (Canton, MI)

MMS Holdings Inc. is a global pharmaceutical service organization (CRO) that focuses on regulatory submission support for the pharmaceutical, biotech and medical device industries. We support pharmaceutical and biotech industries with medical writing, biostatistics, clinical programming, data management, clinical development, regulatory affairs, regulatory submissions and pharmacovigilance. Our mission is to deliver high quality services, rooted in good science and decades of regulatory background, that will assist our clients in developing and marketing life-changing therapies, thereby positively affecting patients' lives worldwide. MMS is looking to expand regulatory services within the US. We are looking to add several regulatory strategists with background in these regions to work with our clients who are planning to run clinical trials, file marketing applications and/or engage in regulatory activities with health authorities in these regions.